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    • 专利摘要:
    The invention is in a series of fluorinated cycloalkanecarboxamides, typically perfluorinated cycloalkanecarboxanilides. The compounds exhibit insecticidal and arachnicidal activity.
    公开号:SU1561822A3
    申请号:SU864027246
    申请日:1986-04-04
    公开日:1990-04-30
    发明作者:Виктор Уренович Джозеф
    申请人:Эр Продактс Энд Кемикалз, Инк. (Фирма)；
    IPC主号:
    专利说明:

     cm
    The invention relates to organic chemistry, namely to a method for producing new carboxanilides of the general formula
    Bi-C-jr-R,
    II
    (one)
    where R, is perfluorodecahidronaphyl, un-decafluorocyclohexyl, decafluorocyclohexyl;
    Ra is phenyl, substituted with pnro group or 2 to 4 independently selected RJ groups,
    where R3 is bromine or chlorine, or two 1 independently selected groups R4, where 1C is iodine, nitro, cyano, trifluoromethyl, or two groups R and R, one of which is methyl, chlorine or bromine, and the other is nitro, methylsulfuryl either fluorosulfonyl, or two groups, one of which is methyl and the other is nitro or fluorosulfonyl, or three groups, two of which are nitro, trifluoromethyl, or chlorine, and a third, bromine, or two groups of chlorine, and a third nitro, or two nitro groups in position 2 and 49 and a third - C, -C-alkoxy or kiltiogroup in position 3 or 5, or three groups, o the bottom of which is methyl, and two groups are independently selected from the series Containing chlorine or nitro, or R2 is naphthyl substituted by two groups representing nitro or bromine, or their ammonium salts, where ammonium has the following formula
    F
    © Rg
    f-rs
    AL
    where is rj. and R6 is each independently alkyl, benzyl, the total number of carbon atoms in all groups of R and R6 being 12-60, or am
    40
    . Calculated,%: C 35.00; H 1.13; N 6.28.
    C13H5FU N2 ° 3Found,%: C 34.91; And 1.10; N 6.48.
    Example 2 -Iodo-4 -niter 1,2,2,3,3,4,4,5,5,6,6-undecafluorose loghexanecarboxanilide, so-called 125-1
    monium salts, which have insecticidal activity and can be used in agriculture.
    The purpose of the invention is to develop an affordable method for producing compounds. The yield is 38%.
    Formula I having a high insecticide; Calculated,%: C 27.35; H 0.70; ticidal activity. N 4,89.
    The invention is illustrated as follows: IN2Og. examples.
    Example 1. 21-Brom-41-yitro 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide.
    1,2,2,3,3,4,4,5,5,6,6-undecafluoro-cshslohexanecarbonyl fluoride of 60% purity (10.9 g; 0.02 mol) and three 50
    Ethylamine (2 g; 0.02 mol) is placed in 25 ml of diethyl ether. Dropwise at ambient temperature (about 25 ° C) is added to 75 ml.
    55
    Found,%: C 27.11; H 0.67; N 4.68.
    Example 4, 2, 4 -Dinitro2, 3; 3,4S4,5,5,6,6-undecafluorocyclo sank arboxanilide, so pl. 106-109 ° C yield of 14%.
    Calculated,%: C, 31.79; H 0.82; N 8.55; F 42.54.
     .
    Found,%: C 32.77; H 0.84; N 9.43; F 43.66.
    simple diethyl ether 2-bromo-4-nitroaniline (11.35 g; 0.02 mol). Then the reaction mixture was stirred for 1.5 hours. Thin layer chromatography showed no aniline starting material. The reaction mixture is washed with water three times and diluted once with sodium bicarbonate solution and then dried. Thereafter
    evaporation of the solvent. The residue of the product is separated by liquid chromatography on silica gel with an acetate: hexane ratio of 1: 5 and
    14.5 g of product are obtained containing the occluded solvent. The product is recrystallized from hexane and air dried, with the result that 5.0 g (48%) of the purified product is obtained, melting at 98-101 ° C. An additional 1 g is obtained from the mother liquor and the total yield is 57%,
    Calculated,%: C 29.74; H 0.77; N 5.34.
    With eH4VgRi YOGOe.
    Found,%: C 30.14; H 0.91; N 5.81.
    Other compounds of the invention obtained in accordance with Example 1 using similar procedures are given below.
    PRI mme R 2. 4 Nitro 1,2,2,3,3, 4,4,5,5,6,6-undecafluorocyclohexane-carboxanilide, so pl. 166-169 With the yield of 67%.
    . Calculated,%: C 35.00; H 1.13; N 6.28.
    C13H5FU N2 ° 3Found,%: C 34.91; And 1.10; N 6.48.
    Example 2-Iodo-4-nitro 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, so-called 125-127 ° C,
    yield 38%.
      IN2Og.
    Found,%: C 27.11; H 0.67; N 4.68.
    Example 4, 2, 4-Dinitro1,2, 2,3; 3,4S4,5,5,6,6-undecafluorocyclohexane arboxanilide, so pl. 106-109 ° C, yield 14%.
    Calculated,%: C, 31.79; H 0.82; N 8.55; F 42.54.
     .
    Found,%: C 32.77; H 0.84; N 9.43; F 43.66.
    51561822
    EXAMPLE 5 2-Chloro-5 nitro 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, mp. 115-118 ° C, yield 24%.
    Calculated,%: C 32.53; H 0.63; N 5.84.
    ,, CgOe.
    Found,%: C 32.50; 32.22; H 0.73; 0.84; N 5.66; 5.62.
    Example 2-Chloro-4-nitro-1,2,2,3, 4,5,5,6,6-undecafluorocyclohexanecarboxanilide, m.p. 90-93 ° C, yield 31%.
    Calculated,%: C 32.48; H 0.83; N 5.82.
    .SZ ..
    Found,%: C 33.60; H 1.01; N 7.32.
    Example 12. 2-Cyano 4-chloro-1,2,2,3,3,4,4,5,5,5,6,6-undecafluorocyclic hexanecarboxanilide, mp. 122-124 ° C. 5 Example 13. 2- (Trifluoromethyl) -4-bromo-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilind m.p. 104 106 ° C.
    Calculated,%: C 30.70; H 0.73; 10 N 2.56.
    C 4H4BrF NO.
    Found,%: C 31.01; H 0.69; N 2.24.
    Etc. and measure 14. 2 /, 3 Dichloro-1,2, 15 2,3,3,4,4,5,5,6,6 undecafluorocyclohexane carboxanilide, mp. 89-91 ° C.
    Example. 2-Methyl-4-nitro-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, m.p. 102- 105 ° C, yield 38%.
    Calculated,%: C, 36.54; H 1.53; N 6.08.
    C HjFflN O ,.
    Found,%: C 43.69; 37.36; H 2.85; 1.72 M 10.44; 6.03.
    Example 2-Methyl-5-nitroP yielding 15. 3,4-Dichloro-1,2,2,3,3,4,4,5,5,6,6-undecaftopi-20 lehexancarboxanilide, t. square 128-132 ° C.
    PRI me R 16. 3.4 Dibromo-1,2, 2,3,3,4,4,5,5,5,6,6-undecafluorocyclohexancarboxanilide, m.p. 126-128 C, 25 yield 39%.
    Calculated,%: C 27.93; H 0.72; N 2.51.
    SiN4Vg4R „N0.
    Found,% i C 28.15; H 0.86; 1,2,2,3,3,4,4,5,5,6,6-undecafluorcyclo-ZO N 2.77.
    hexanecarboxanilide, so pl. 107-109 ° C, Example 17. Zr-Chloro-4 fluorofluoride 33%.
    1,2,2,3,3,4,4,5,5,6,6-undecafluoronic-lehexancarboxanilide, so pl. 147-149 ° C, yield 9%.
    Calculated,%: C, 36.54; H 1.53; N 6.09.
    (NZ03.
    Found %: C, 36.66; H 1.28; N 6.19.
    Example 9 21. 21 Niano-4-nitro 1,2,2,3,3,4,4,5,5,5,6,6-undecafluorocyclohexanecarboxanilide, m.p. 119-120 ° C, yield 20%.
    Calculated,%: C 35.69; H 0.86; N 8.92.
    WITH ,
    "
    Found %: C, 35.94; H 1.13; N 8.66.
    Example 10. 2- (Trifluoromethyl) -4-nitro-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, mp. 80-81 ° C, yield 34%.
    Example 11. 2 (-Fluoro-5-nitro 1,2,2,3,3,4,4,5,5,5,6,6-undecafluorocyclohexancarboxanilide, mp 101–102 ° C, yield 43 %
    Calculated,%: C 33.71; H 0.65; N 6.05;
    From “N 14YG03.
    Found,%: C 33.56; H 0.66; N 6.05.
    Example 12. 2-Cyano 4-chloro-1,2,2,3,3,4,4,5,5,5,6,6-undecafluorocycle - hexanecarboxanilide, so pl. 122-124 ° C. Example 13. 2 - (Trifluoromethyl) - 4-bromo-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilind m.p. 104 106 ° C.
    Calculated,%: C 30.70; H 0.73; N 2.56.
    C 4H4BrF NO.
    Found,%: C 31.01; H 0.69; N 2.24.
    Etc. and measure 14. 2 /, 3 Dichloro-1,2, 5 2,3,3,4,4,5,5,6,6 undecafluorocyclohexane carboxanilide, m.p. 89-91 ° C.
    PRI me R 15. 3,4-Dichloro-1,2,2,3,3,4,4,5,5,5,6,6-undecaphtopi Csh-lo-hexane-carboxanilide, m.p. 128-132 ° C.
    PRI me R 16. 3.4 Dibromo-1,2, 2,3,3,4,4,5,5,5,6,6-undecafluorocyclohexancarboxanilide, m.p. 126-128 ° C, yield 39%.
    Calculated,%: C 27.93; H 0.72; N 2.51.
    SiN4Vg4R „N0.
    Found,% i C 28.15; H 0.86; N 2.77.
    five
    0
    1,2,2,3,3,4,4,5,5,6,6-undecafluoronic-lehexancarboxanilide, so pl. 147-149 ° C, yield 9%.
    Calculated,%: C 34.42; H 0.89; N 3.09.
    .S1P, 2 N0.
    Found,%: C 34.30; H 0.99; N 3.15.
    0 Example 18.., 5 -Dibromo-1,2, 2,3,3,4,4,5,5,5,6,6-undecafluorocyclohex-sangg rboxanilide, m.p. 110-113 ° C, yield 24%.
    Calculated,%: C 27.93; H 0.72; 5 N L., 50; Br 28.59; F 37.38.
    Cr, H4Br2F, NO.
    Found,%: C 28.09; H 0.66; N 2.52 ;, Br 28.77; F 37.54.
    Example 19. 2, b-Dichloro-1,2, 2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, m.p. 159-162 ° C, yield 27%.
    Calculated,%: C 33.21; H 0.85; N 2.97; C1 15.08; F 44.46.
    C, 4H4C1,, Pc NO.
    Found,%: C 33.04; H 0.85; N 2.90; C1 14.99} F 44.59.
    PRI me R 20.. , 5-dichloro-1,2, 2,3,3,4,4,5,5,6,6-undecafluorocyclo5
    hexanecarboxanilide, mp, 90-101 ° C, BB1IND 26%.
    Calculated,%: C 33.21; H 0.85; N 2.97; C1 15.08; F 44.46.
    SvN4S1gG „N0.
    Found,%: C 33.30; H 0.97; N 3.00; C1 15.12; F 44.51.
    EXAMPLE 21: 2.4 Dichloro-1,2, 2,3,3,4,4,5,5,5,6,6-undecafluoro-diclohexanecarboxanilide, mp. 83-85 ° C, yield 8.5%.
    Calculated,%: C 33.21; H 0.85; N 2.97; C1 15.08; F 44.26.
    G0H4C1ZF NO.
    Found,%: C 33.30; H 0.85; N 3.04; C1 15.32; F 44.24.
     Example 22. 3;, 5-Dichloro-1,2 2,3,3,4,4,5,5,6,6 undecafluorocyclo o hexanecarboxanilide, m.p. C, yield 25%.
     Calculated,%: C 33.21; H 0.85; N-2.97; C1 15.08; F 44.46;
    CtftUCUF NO.
    Found,%: C 33.25; H 0.81; N 3.02; Cl 15.30j F 44.67.
    PRI me R 23.. , b - DibromoM, 2, 2.3 S3,4,4,5,5,6, b-undecafluorocyclohexanecarboxanilide, m.p. 143-145 C.
    EXAMPLE 24, 21, 4 -Dibromo-1, 2, 2,3,3,4,4,5,5,6,6-undecafluorocyclohexancarboxanilide, m.p. 84-86 ° C.
    PRI mme R 25. 4 Chloro-2-nitro 1,2,2,3,3,4,4,5,5,6,6 undecafluorodicolexancarboxanilide, mp, 66-69 C, yield 35%.
    Calculated,%: C 32.49; H 0.84; N 5.83.
     .
    Found %: C 33.09; H 0.97; N 6.37.
    PRI me R 26. 3 -Nitro-4-chloro-1,2,2,3,3,4,4,5,5,6,6-undec aptor-cyclohexanecarboxanilide, mp. 118- 121 ° C, yield 67%.
    Calculated,%: C 32.50; H 0.83; N 5.83.
      ,
    Found,%: C 32.71; H 1.02; N 6.10. ((
    PRI me R 27. 3-Chloro-4-nitro 1,2,2,3,3,4,4,5,5,6,6-undec acyclocyclohexanecarboxanilide, mp, 141- 144 ° C, yield 23%.
    Calculated,%: C 32.49; H 0.84; N 5.83.
    C „H4C1F, N, 103- Found: C 32.67; H 1.05; N 5.89.
    II p and mep 28, 3,5-dinitro-1,2,2 3,3,4,4,5,5,6,6-undecafluorocyclohexancarboxanilide, so pl. 140-143 ° C, yield 22%.
    Calculated,%: C, 31.79; H 0.82; N 8.55.
    C ,, H4FM,.
    Found,%: C 31.61; H 0.79; N 9.01.
    EXAMPLE 29 2,5-Dinitro 1,2, 2,3,3,4,4,5,5,5,6,6 Undecafluorocyclohexancarboxanilide, m.p. 125-128 ° C.
    EXAMPLE 30 Sx, 4-Dinitro-1,2, 2,3,3,4,4,5,5,6,6-undecafluorocyclohexancarboxanilide, m.p. 118-121 ° C.
    PRI me R 31. 2,6 -Difrro-1,2 2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, etc. 88-90 C.
    PRI me R 32. C - (Trifluoromethyl) - 4-chloro-1,2,2,3,3,4,4,5,5,6,6,6-undecaphthorocyclohexanecarboxanilide, m.p. 114-116 ° C.
    Example 33. 2-Chloro-5 - (trifluoromethyl) -1,2,2,3,3,4,4,5,5,6,6-un-decafluorocyclohexane carboxanilide, mp. 81-84 ° C, yield 51%.
    Calculated,%: C 33.50; H 0.80; N 2.79.
    C 4H4C1RNJ.
    Found,%: C 33.69; 33.51; H 0.84; 0.89; N 2.60; N 2.59.
    Note ep 34. 3,5-bis (Trifluoromethyl) -1, 2,2,3,3,4,4,5,5,6,6 -undecaf torcyclohexanecarboxanilide, t.p.T. 137-139 ° С, yield 29%.
    Calculated,%: C 33.55; H 0.75; N 2.61.
    C, 5H + F17NO.
    Found,%: C 33.80; H 0.51; N 2.79.
    PRI me R 35.. -Nitro-4-cyano-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, m.p. 153-154 ° C.
    Calculated,%: C 35.70; H 0.85; N 8.92.
    CH4H4F. "
    Found,%: C 36.20; H 0.67; N 8.59.
    Example -Nitro-4 - (triftbrmethyl) -1,2,2,3,3,4,4,5,5,6,6-un-decafluorohexanecarboxanilide.
    Calculated,%: C 32.80; H 0S78; S 5.45.
    C, 4H4F 4N103.
    Found,%: C 32.77; H 0.70; N 5.59.
    9 156182210
    Example 2-Methyl-4-bromo-C 4H7FMN203.
    1,2,2,3,3,4,4,5,5,6,6-undecafluorcic-Found,%: C 37.29; H 1.86;
    Helexanecarboxanilide, m.p. 97-99 C, N 6.73.
    yield 17%. cExample 45. 3 -o-4-methyl -Calculated,%: C 34.00; H 1.42; 1,2,2,3,3,4,4,5,5,6,6,6-undecafluorcycNN 2.84.hexanecarboxanilide, m.p. 118C 4H7BrF NO .120 ° SL yield 14%.
    Found,%: C 34.07 :, H 1.31; Calculated,%: C 38.83; H 1.67;
    N 2.60. (10 N 3.24.
    Example 38 2-Bromo-4-methyl-C (4H7F12NO.
    1,2,2,3,3,4,4,5,5,6,6-undecafluorcic-Found%: C 38.83; 39.25;
    Helexanecarboxanilide, m.p. 79-80 ° C.N. 1.71; 1.74; N 3.02; 3.09.
    PRI me R 39. 3-Chloro-4 -methyl-II p and meper 46. 3-Methyl-4-fluoro1, 2,2,3,3,4,4,5,5,5,6, 6-undecaf.ordic-J5 1 G2 2,3,3,4,4,5,5,6,6,6-undecafluorocyclohexanecarboxanilide, m.p. 108-lelexanecarboxanilide, m.p. 123-
    110 ° C. 125 ° C, yield 34%.
    PRI and M R p 40. 2G-Methyl-5-chloro-Calculated,%: C 38,83; H 1.63;
    1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclo-N 3.24.
    hexanecarboxanilide, so pl. 115-118 C, 20 C {4-H7F1ZNO.
    yield 11%. Found,%: C 38.84; H 1.68;
    Calculated,%: C 37.45; H 1.57; N 3.04.
    S 3.12. Example 47.. -Methyl-5 -fluorCHH7C1F, NO.1,2,2,3,3,4,4,5,5,6,6-undecafluorocyte Found,%: C 37.57; H 1.52; 25 logex carboxanilide, so pl. 105N 2.91.108 ° C, yield 46%.
    II p and mep 41. 2G-Methyl-4-chloro-Calculated,%: C 38.83; K 1.63;
    1,2,2,3,3,4,4,5,5,6,6-undecafluorcic-N 3.24.
    Helexanecarboxanilide, m.p. 75-78 C, GMO.
    yield 31% .30 Found: C 38.93; H 1.49 ;,
    Calculated,%: C 37.45; H 1.57; N 3.07.
    N3.12. Example 48. 2-Methyl-3-fluoroC 4 H7 GIF f NO. 2,3,3,4,4,5,5,6,6-undecafluorine Found,%: C 37.50, H 1.47; .lohexanecarboxanilide, m.p. 124N 2.89. , 35 126 ° С, yield 50%.
    PRI me R 42. 2 -Metil-z-chloro-Calculated,%: C 38,82; H 1.63;
    1,2,2,3,3,4,4,5,5,6,6-undecafluorcic-N 3.23.
    Helexanecarboxanilide, mp, 115.
    116 ° C, yield 32%. Found,%: C 38.77; H 1.46;
    Calculated,%: C 37.40; H 1.57; 40 N 3 20N3, 11.-Example 49.. , 5 -Dichloro-4 С 4Н7С1Р „N0. Nitro-1, 3,3,4,4,5,5,6,6-undec-
    Found,%: C 37.51; H 1.47; fluorocyclohexanecarboxanilide, m.p.
    N 3.10. / 99-100 ° C, yield 7%.
    Example 43. 2 / -chloro-5 -methyl-45 Calculated,%: C 30.32; H 0.59;
    1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclo-N 5.44.
    hexanecarboxanilide, so pl. 55-58 C, C, N20 ,. yield 77%.
    Calculated,%: C 37.45; H 1.57; . Found,%: C 30.31; H 0.85;
    N 3.1250 N 5.33.
    CHH7C1F and N0. Example 50. 2-Methyl-4-nitro. Found,%: C 37.82; H 1.42; 5-chloro-1,2,2,3,3,4,4,5,5,6,6-unde .N 3.29 kafluorocyclohexanecarboxanilide
    PRI me R 44. 2 -Citro-4 -methyl-154-156 ° C, yield 33%.
    1,2,2,3,3,4,4,5,5,6,6-undecafluorcine-.55 Calculated,%: C, 33.99; H 1.22;
    Helexanecarboxanilide, m.p. 96-98 C, N 5.66.
    yield 40% .C HgClF ,, H40z.
    Calculated,%: C, 36.54; H 1.53; Found: C 34.18; H 1.41;
    N 6.08. N 5.56.
    PRI me R 51. 2, 5 Dichloro-4 bromo-1,2,2,3,3,4,4,5,5,6,6-undec-fluorocyclohexanecarboxanilide, m.p. 128-129.5 ° C.
    Calculated% C 28.42; H 0.55; N 2.55.
    With H3BrClЈF MNO.
    Found,%: C 28.48; H 0.76; N 2.80.
    Example 52. 21, 4.5-Trichloro-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, m.p. 127-128.5 ° C.
    Calculated,%; C 31.00; H 0.60; N 2.80.
    C, 3H, CiBF ,, N0.
     Found,%: C 30.99; H 0.61; N 2.82.
    Example 53. 2,4-Dinitro b chloro-1,2,2,3,3,4,4,5,5,5,6,6-undec-fluorocyclohexanecarboxanilide, mp. 109-111 ° C.
    Example 54. 2 -Iitro-4, 6-di chloro-1,2,2,3,3,4,4,5,5,6,6-undec-fluorocyclohexanecarboxanilide, mp. 95-97 ° C. f
    EXAMPLE 55 2,4-Dynitro-5-fluoro-1,2,2,3,3,4,4,5,5,6,6-undec-fluorocyclohexanecarboxanilide,. 126-128 ° C.
    Example 56. 2, b-Dichloro-4 - nitro-1,2,2,3,3,4,4,5,5,6,6-undec-fluorocyclohexanecarboxanilide, mp. 155-157 ° C.
    PRI me R 57. 2.4 (b-Trichloro 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexancarboxanilide, mp 170-172 ° C, yield 39%.
    Calculated,%: C 30.98; H 0.60; N 2.78.
    With “NESTR” “N0.
    Found,%: C 30.97; H 0.52; N 2,55.f
    PRI me R 58. 3,5-Dichloro-4 - bromo-1,2,2,3,3,4,4,5,5,6,6-undec-fluorocycle oghecanar boxanilide, m.p. 1 71-1.2,5 ° C.
    Calculated,%: C, 28.44; H 0.55; N 2.55.
    C „N VgS14R N0. Found, / „: С 28, Ь5; H 0.81; N 2.67.
    EXAMPLE 59 2,4f, 6 -Tribromo 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexancarboxanilide, mp. 115 -
    117 ° C.
    Example hO. 3fX, 5-Trichloro 1,2,2,3,3,4,4,5, b, b, 6-undecafluorcic
    0
    five
    0
    five
    0
    - Nitro-4, 6 logexcancarboxanilide, so pl. 152-154 ° C.
    Example 61. 2
    dichloro-1,2,2,3,3,4,4,5,5,6,6-undec-fluorocyclohexanecarboxanilide, m.p. 97-99 ° C.
    Example 62. 2-Bromo-4 - (trifluoromethyl) -1,2,2,3,3,4,4,5,5,6,6-un-decafluorocyclohexanecarboxanilide.
    Calculated,%: C 29.12; H 0.56; N 10.45; F 38.98.
    With „Н3РН N407.
    Found,%: C 30.37; H 0.63; 5 N 10.9 e; F 33.79.
    Example 63. 2, l-Dinitro-4 (trifluoromethyl) -1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, the yield of the crude product is 61%, m.p. after recrystallization 173-175 ° C.
    Calculated,%: C 30.07; H 0.54; N 7.51.
    Cl4H, F1 tN3Off.
    Found,%: C 30.59; H 0.40; N 7.43.
    PRI me R 64. 2, 3, 4, 5 -Tetra-chloro-1,2,2,3,3,4,4,5,5,6, b-undec a-fluorocyclohexanecarboxanilide, mp . 130 ° C, yield 19%.
    Calculated,%: C, 28.97; H 0.37; N 2.60.
    CjjEtCl Frt NO.
    Found,%: C 29.21; H 0.60; N 2.77.
    EXAMPLE 65 2.3, 4.5 -Tetra-fluoro-1,2,2,3,3,4,4,5,5,6,6-undec-fluorocyclohexanecarboxanilide, m.p. 55-59 ° C, yield 18%.
    Calculated,%: C 33.01; H 0.42; N 2.96.
    C43H4P 5NO.
    Found,%: C 33.72; H 0.51; N 2.90.
    PRI me R 66.. 3,5f, b -Tetra-fluoro-1,2,2,3,3,4,4,5,5, b, 6-undecaphortcyclohexanecarboxanilide, m.p. 115 117 ° C, yield 38%.
    Calculated,%: C 33.01; H 0.42; N 2.96.
    , 5-NO.
    Found,%: C 32.79; H 0.48; N 2.69.
    PRI me R 67: 2, 3,4,5, b - Pentafluoro-1,2,2,3,3,4,4,5,5,6,6 - undecafluorocyclohexanecarboxanilide, so pl. 135 ° C, yield 19%.
    Calculated,%: C 31.80; H 0.21; N 2.85.
    five
    0
    five
    CWHF, 6 NO.
    Found,%: C 31.65; H 0.11; N 2.63.
    EXAMPLE 68: 2,354.5, Pentachloro-1,2,2,3,3,4,4,5,5,6,6- undecafluorocyclohexanecarboxanilide, mp. 181-184 ° C, yield 38%,
    PRI me R 69. M - (5-Nntro-2 pi dil) -1,2,2,3,3,4,4,5,5,6, ekafto cyclohexanecarboxanilide, mp. 110-112 ° C, 24% yield.
    Calcd.: C, 32.29; H 0.89; N 9.35.
    CuH, FHN2Ov.
    Found,%: C 32.16; 32.27; H 0.74; 0.84; U 9.22; 9.23.
    PRI me R 70. 2 Bromo-4-nitro 4- (trifluoromethyl) -1,2,2,3,3,4,4,5,5,6 6-undecagulation cyclohexanecarboxakilid m.p. 102-104 ° C, yield 1.7%.
    Calculated, ;;: C, 29.24; H 0.70; N 4.87.
    C, 4Н4ВгР ,, CgOe.
    Found,%: C 29.53; H 0.44; N 4.83.
    Example 71. A mixture of 2 bromo 4 nitro-4- (trifluoromethyl) -1,2,2,3,3,4,4 5,5 j 6,6 -decafluorocyclohexanecarboxanilide and 2-bromo-4 -nitro x, x - bis (trifluorometh yl) gx, x, x, x, x, x, tafluorcyclopentanecarboxanilide, mp 93-95 ° C, yield 10%.
    Calculated,%: C, 29.24; H 0.70; N 4.87.
    .H4BrF ,, NZ0V
    Found,%: C 29.11; H 0.74; N 4.96.
    Example 72. M-Methyl-2g-bromo-4-nitro 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide.
    2 -Bromo-4-nitro-1,2,2,3,3,4,4, 5,5,6,6-undecafluorocyclohexanecarboxanilide (5.0 g, 0.24 mol) and methyl iodide (15 ml , 0.24 mol) is mixed in 40 ml of acetone and the reaction mixture is stirred for 60 hours. The reaction mixture is added with about 200 ml of water, and then this mixture is extracted with simple ether, dried, evaporated and separated by chromatography silica gel with an ethyl acetate-tgpentane ratio of 1: 4. Thin-layer chromatography showed one spot with a lower than that of the starting cyclohexane carboxanilide Rf, which indicates the conversion of N-methyl-2-bromo-4-nitro-1,2,2,3,3,4,4 to the target, 5,6,6-unde
    five
    ABOUT
    five
    0
    0
    five
    0
    five
    Kafluorocyclohexanecarboxanilide. The yield is 2.5 g of oil (49%).
    Calculated,%: C 31.19; H 1.12; N 5.20.
    C, 4H6BrF, Hg0e.
    Found,%: C 31.46; H 0.82; N 5.21.
    Example 73. 2-Bromo-4-nitro-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, sodium salt,
    2 / Bromo-4 Nitro-1,2,2,3,3,4,4, 5,5,6,6-undecafluorocyclohexanecarboxanilide (2.6 g, 0.005 mol) and sodium hydroxide (0.2 g, 0.005 mol) is mixed in 60 ml of acetone at room temperature of about 25 ° C. All volatiles and water are removed by evaporation. The solid residue is dissolved in hot toluene-ethyl acetate. The product does not crystallize, but forms chunks. They are isolated and dried under vacuum. The yield is 2.1 g (77%), so pl. 200 ° C, with decomposition.
    Calculated,%: C, 28.54; H 0.55; N 5.12.
    С1 Н3ВгР „N203Na.
    Found,%: C 28.84; H.1,10; N 4 „90.
    PRI me R Ik. 2-Bromo-4-nitro 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyc-, lehexanecarboxanilide, tetraethylammonium salt.
    2 Bromo-4-nitro-1,2,2,3,3,4,4, 5л5,6,6 undecafluorocyclohexanecarboxanilide (2.6 g. 0.005 mol) is dissolved in 25 ml of acetone and 2N. Sodium hydroxide (052 g, 0.005 mol) is added in one portion. Tetraethylammonium bromide (1.1 g, mol) is then added and the reaction mixture is stirred until it becomes a single phase. The reaction mixture is poured into water / ice, -stripped with methylene chloride / brine, dried over magnesium sulphate and evaporated, NMR showed a mixture of the target salt and classification substance, Resid. stolen with acetone, further treated with sodium hydroxide and tetA; raethylammonin bromide and treated as described above. Yield 1.5 g (.46 / 0 2 -bromo-4 -nitry- T, 3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, tetraethylammonium salt as an oil.
    Note 75. 2 -Bromo-4-nitro-, 3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, tetra n-propylammonium salt.
    2-Bromo 4-nitro-1,2,2,3,3,4,4, 5,5,6 6-undecafluorocyclohexanecarboxanilide (236 g, 0.005 mol) is dissolved in 50 ml of acetone and added in one portion 1 n. sodium hydroxide (5.0 ml, 0.005 mol}). Then tetrapropylammonium bromide (1.35 g, 0.005 mol) is delivered and the reaction mixture is stirred until it becomes one phase. Then the reaction mixture is poured onto ice / water and the oily residue is separated, extracted with diethyl ether, dried over magnesium sulphate and crystallized at -10 ° C from water - ethanol to give 0.9 g (25%) of the tetra-n-propylammonium salt, m.p. -87 4
    Using the same procedure as in the above two examples, the following additive salts are obtained. The identity of the salts is verified by NMR.
    Example 76 2-Bromo-4-nitro 1,2,2,3,3,4,4,5,5,5,6,6 undecafluorocyclohexanecarboxanilide, tri-n-butylmethylammonium salt, etc. 129-130 ° C, yield 56%.
    Calculated,%: C 42.00; H 4.72; N 5.65.
    Ce6H3 BrFM NZ0 ,.
    Found,%: C 43.02; H 4.51; N 62.2.f
    Example 77 2-Bromo-4-nitro 1,2,2,3,3,4,4,5,5,5,6,6-undecafluorocyclohexancarboxanilide, tetra-n-butylammonium salt, m.p. 94-97 C, yield 94%.
    Calculated,%: C, 44.40; H 5.27; N 5.36.
    C qH-jh VZGg
    11 N403ngo.
    Found,%: C D4,66; H 5.03; N 5.46. (;
    Example78. 2 Bromo-4-nitro 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, tetra-n-pentylammonium salt, m.p. 80-81 ° C, yield 85%.
    Calculated,%: C, 47.11; H 5.76; N 5.00.
    C3, H, 8BrFM N40y H40.
    Found,%: With 47.46; H 5.61; N 4.79.,
    PRI me R 79. 2 (Bromo-4-nitro 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, tetra-n-hexylammonium salt, oil, yield 53%.
    Calculated,%: C 49.56; H 6.41; N 4.69.
    50
    five
    0
    With „Н5ЈГВгР
    , “NZ0, - NgO.
    Found,%: C 51.38; H 6.73; N4.75.
    Example 80 2-Bromo-4-nitro 1,2,2,3,3,4,4,5,5,5,6,6-undecafluorocyclohexanecarboxanilide, tetra-n-heptylammonium salt, oil, yield 51%.
    Calculated,%: C, 51.68; H 6.88; 4.41.
    C4tH6, BrFw, - HZ0.
    Found,%: C 53.21; H 7.17; 4.29.
    EXAMPLE 81. 2; -Bromo-4-nitro-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, benzyltriethylammonium salt, t. square 77-82 ° C, 77% yield.
    Calculated,%: C 42.44; H 3.67; N 5.71.
    C26HiSrBrF,.
    Found,%: C 41.79; H 2.90; N 5.85. I
    Example 82 2-Bromo-4g -nitro-1,2,2,3,3,4,4,5,5,6,6-undecafluoro-cyclohexanecarboxanilide, hexadecyltrimethylammonium salt, m.p. 53-55 ° C, yield 60%.
    Calculated,%: C 46.50; H 5.73; N 5.08.
    C3 H45BrF ", N40, -HtO.
    Found,%: C 47.57; H 4.84;
    5 N.
    Example 83. 2 — Bromo-4-nitro1, 2,2,3,3,4,4,5,5,5,6,6-undecafluorocyclohexancarboxanilide, octadecyltrimethylammonium salt, m.p. 48-53 ° C, 0 yield 38%.
    Calculated,%: C, 47.78; H 6.01; N 4.92.
    C, 4H (jBrFM H40. Found: C, 47.54; H, 5.83; 5 N, 4.74.
    Example 84. 2-Bromo-4-nitro 1,2,2,3,3,4,4,5,5,6,6,6-undecafluorocyclohexanecarboxanilide, benzyl-tri-n-butylammonium salt, oil, yield 42 % n Calculated,%: C 47.59; H 4.78; N 5.24.
    .Н37 BrF «N20-5- Н40.
    Found,%: C 49.97; H 5.70; N 4.90.
    5 Example 85.2-Bromo-4-nitro1, 2,2,3,3,4,4,5,5,6,6-ndecafluorocyclohexancarboxanilide, dimethyl bis salt (, c) ammonium, oil, yield 39%.
    171561822
    EXAMPLE 86 2 -Bromo-4-nitro1 l g
    1,2, 2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, methyltri-n-octylammonium salt, oil, 53% yield.
    Calculated,%: C 50.17; H 6.43; N 4.62.
    С38Н57Вг Мг03.Н „0.
    Found%: C 50.47, H 6.63, N 4.34 f
    Example 87, 2-Bromo ™ 4 -nitro 1,2,2,3,3,4,4,5,5,5,6,6-undecafluorcyclohexanecarboxanilide, methyltris (C5-C10) ammonium salt, oil, yield 45%
    PROMER 88: 2 Bromo 4 -nitro 1,2,2,3,3,4,4S5,5,6,6-undecafluorocyclohexanecarboxanilide, dimethyl-6c (i10-C1J) ammonium salt, salt in the form of oil, yield 37%.
    Example 89. 2-Chloro-4-nitro-1,2,2,3,3,4,4,5,5,5,6,6-undecafluorocyclohexanecarboxanilide, tetra-n salt of ammonium sulfate, t, pl. 65-69 ° C, you-; a stroke of 52%.
    Calculated,%: C 43.90; H 4.86; N 6.14.
    C45HMC1F4, HJ03
    NgO.
    Calculated,%: C 50.43; H 6.30; N 5.19;
    C54H ,, 9С1РИ M, Oe-NgO,
    Found,%: C 52.35; H 7.50;
    Found,%: C 43.88; H 4 „61; N 5.99.
    PRI me R 90. 2-Chloro-4-nitro 30 N,
    1,2,2,3,3,4,4,5,5,6,6-undecafluorcic Example 96. 2-Chloro-4-nitro1, 2,2,3,3,4,4,585,6,6 -undecafluorocyclohexanecarboxanilide, tetra-nbutylammonium salt, m.p. 107-109 ° С, yield 80%.
    Calculated,%: C 47.06; H 5558;
    N 5.68.
    C HyjClF NjOy HЈ0.
    Found,%: C, 47.08; H b, 34; N 5.87.
    35
    Helexanecarboxanilide, methyl-TpHC- (Cg-C10) ammonium salt, oil, yield 26%.,
    EXAMPLE 97. 2-Chloro-4-nitro-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, methyltri-n-octylammonium salt, oil , yield 48%.
    PRI me R 91. 2-Chloro-4 -nitro-40 Calculated,%: C, 52.72; H 6.82; 1,2,2,3,3,4,4,5,5,6,6-undecafluorcic-N.
    Helexanecarboxanilide, tetra-n- and N, 0 salt, pentylammonium, m.p. 68 - 70 ° C, you- Found,%: C 55.83; H 7.45; move 88%. N 4 30Calculated,%: C 49.78; H 6.20; 45 N 5.28.
    C3, H47ClFt N2U, - H20.
    PRI me R 98. 2,5-Dichloro-4 - nitro-1,2,2,3,3,4,4,5,5,6,6-undec-fluorocyclohexanecarboxanilide, tetra 6-propylammonium salt, m.p. 124-125 ° C; yield 91%.
    Found,%: C 52.59; H 7.29; N 5,52.50
    PRI me R 92. 2-Chloro-4-nitro-1,2,2,3,3,4,4,5,5,6,6-undecafluoroznc-loexancarboxanilide, tetra-n-hexylammonium salt, oil , yield 64%.
    Calculated,%: C 52.51; H 6.07; 55
    N 4.97.
    C51H55C1FH N, 0, - H20.
    Found,%: C, 51.88; H 6.98; N 4.77.
    18
    0
    PRI me R 93. 2-Ch oro-4 -nitr-1,2,2,3,3,4,4,5,5,6,6-undecafluorcyc lehexanecarboxanilide, tetra-n-heptylammonium salt, oil , yield 40%.
    Calculated,%: C 54.21; H 7.21; N 4.63.
    C41H6, ClFf1 Nf30, -H40.
    Found,%: C 54.14; H 7.39; N 4.72.
    Example94. 2-Chloro-4-nitro 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, hexadecyltrimethylammonium salt, m.p. 58-60®С, vkod 50%.
    Calculated,%: C 49, T4; H 6.06; N 5., 37.
    C92.HS6C1F “N30, .H40.
    Found,%: C 49.42} H 5.85; N 5.44.
    Pr cme p 95. 2-Chloro-4-nitro 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, salt of octadecyltrimethylammonium, m.p., 57- 59 ° C, 5 yield of 60%.
    Calculated,%: C 50.43; H 6.30; N 5.19;
    C54H ,, 9С1РИ M, Oe-NgO,
    Found,%: C 52.35; H 7.50;
    0
    0 N,
    Helexanecarboxanilide, methyl-TpHC- (Cg-C10) ammonium salt, oil, yield 26%.,
    EXAMPLE 97. 2-Chloro-4-nitro-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, methyltri-n-octylammonium salt, oil , yield 48%.
    PRI me R 98. 2,5-Dichloro-4 - nitro-1,2,2,3,3,4,4,5,5,6,6-undec-fluorocyclohexanecarboxanilide, tetra 6-propylammonium salt, m.p. 124-125 ° C; yield 91%.
    Calculated,%: C 41.80; H 4.49; N 5.85.
    CWHWOC F4 "N, 0, -. . Found,%: C 42.03; H 4.21; N 5.86.
    Example 99 2, 4-Dnnitro-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, tetra-n-propylammonium salt, oil, yield 63%.
    Calculated,%: C 43.22; H 4.76; N 8.07.
    C25H31FffN, CVHЈ0.
    Found,%: C 43.51; H 4.41 $ 5
    N 8.34.
    Example 100. 2- (Trifluoromethyl) "4-nitro-1,2,2,3,3,4,4,5,5,6, b-undecafluorocyclohexanecarboxanilide, tetra-n-propylammonium salt, oil,
    move 21% .f
    Example 101. 2-Cyano-4-nitro-1, 2,2,3,3,4,4,5,5,5,6,6-undecafluoro-cyclohexanecarboxanilide, tetra-n-propylammonium salt, m.p. 110-112 ° C, 1 yield 77%.
    Calculated,%: C 46.29; H 4.89; N 8.31.
    C26HMF ,, N40VH20 /
    Found,%: C 47.47; H 4.73; 2 N 8.51.
    A microanalysis showed that the product was a mixture of a classification substance and a salt.
    EXAMPLE 102 2 Methyl-4-nit-2-ro-5-chloro-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, tetra salt n-propylammonium , yield 34%.
    Calculated,%: C, 44.74; H 5.05; N 6.02.3
    СГбН „С1Р„ N30. NgO.
    Found,%: C 43.95; H 4.23; N 5.70.
    Example 103. 2-Cyano-4-chloro-1,2,2,3,3,4,4,5,5,5,6,6-undecafluorcic 3 Lehexancarboxanilide, Hexadeg-methyltrimethylammonium salt, mp 100-102 ° C , yield 90%.
    Calculated,%: C 52.00; H 6.22; N 5.51.4
    SMN „5С1Р„ N, 0- HZ0.
    Found,%: C 52.98; H 5.75; N 5.41.
    Example 104 2, 4-dinitro-1,2,2,3,3,4 $ 4,5,5,6,6-undecafluorocyc-4-lexancarboxanilide, hexa-decyltrimethylammonium salt, oil, yield 40%.
    Calculated,%: C 48.48; H 5.98; N 7.07.

    N405 H ,, 0.
    4, N4i5-p4i.50
    Found,%: C 48.27; H 5.79; N 6.86.
    Example 105: 2.41, 5-Trichloro-1,2,2,3,3,4,4,5,5,6,6-undecafluoro-cyclohexane-carboxanilide, hexade methyltrimethylammonium salt, m.p. 85-88 ° C, yield 4%.
    Calculated,%: C 47.68; H 5.75; N 3.48
    55
    0
    five
    0
    five
    0
    five
    0
    five
    ,, NZ0 H40.
    Found,%: With 47.44; H 5.95; N 3.29.
    Example 106 2.4, b-Trichloro-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, hexadecyltrimethylammonium salt, oil, yield 6%.
    Calculated,%: C 47.68; H 5.75; N 3.48.
    SzgN44S13R „YOGO-N ,, 0.
    Found,%: With 47.33; H 5.82; N 3.44.
    Example 107. 2-Methyl-4-nitro-5-chloro-1,2,2,3,3,4,4,5,5,6,6- undecafluorocyclohexanecarboxanilide, hexadecyltrimethylammonium salt, m.p. 75-77 ° C, yield 66%.
    Calculated,%: C 49.78; H 6.20; N 5.28.
    C3, H47C1F “N, 09- H20.
    Found,%: C 49.56; H 5.90; N 5.25.
    Example 108 2,3,4,5-Tetrachloro-1,2,2,3,3,4,4,5,5,5,6,6-undecutorclocyclohexanecarboxanilide, octadecyltrimethylammonium salt, m.p. 65-68 ° C, yield 17%.
    Calculated,%: C 47.02; H 5.69; N 3.23.
    , 7С14Р „NtO -HjjO.
    Found,%: C 44.90; H 5.16; N 3.18.
    Example 109. 2 -Bromo-4-nitro 1,2,2,3,3,4,4,5,5,5,6,6-undec-4-cyclo-cyclo-hexane-carboxanilide, tri-n-butylammonium salt, m.p. 74-71 ° C, yield 63%.
    Calculated,%: C 42.25; H 4.37; N 5.91.
    C42H50BrFM N503.
    Found,%: C 41J95; H 4.24; N 5.80.
    Example 110. A mixture of 21-bromo-4f-nitro-1,2,2,3,3,4,4,5,5,6,6,6-udecafluorocyclohexanecarboxanilide and 2 - bromo-4-nitro-x- (triAtromethyl ) -x, x, x, x, x, x, x, x-octafluorocyclopentanecarboxylicide.
    2 -Bromo-4-nitro-1,2,2,3,3,4,4, 5,5,6,6-acdefluorocyclohexanecarboxyanide is prepared from 1,2,2,3,3,4,4, 5 , 5,6,6-undecafluorocyclohexanecarbonyl fluoride and recrystallized from toluene. The toluene stock solution is evaporated to half the original volume. The product is recrystallized and selected21.
    lt are The toluene stock solution is separated by chromatography on silica gel with toluene and then recrystallized from toluene, m.p. 85-82 ° C, yield 19%.
    Calculated,%: C 29.74; H 0.77; N 5.34.
    C, 3H4BrF, N203.
    Found,%: C 29.67; H 0.60; N 5.48.
    f4
    F-NMR showed that the product consisted of approximately 66% 21-bromo-4 -nitro-1,2,2,3,3,4,4,5,5,6,6-nNafafluoro-cyclohexanecarboxanilide and approximately
    33% 2-bromo-nitro-x-Striftormethyl-x, x, x, x, x, x, x, x-octafluorocyclopentanecarboxayilide.
    Other representative compounds are listed below. Unless otherwise stated, each compound is from using the procedures described in example 1 or in examples 74-75.
    Example 111. 2 -Nitro 4 -carboethoxy-1,2,2,3,3,4,4,5,5,6,6-unde cafluorocyclohexanecarboxanilide, mp 74-76 ° C.
    Calculated,%: C 37.06; H 1.74; N 5.40.
    CteHjFuN Oj ..
    Found,%: C 36.66; H 1.78; N 5.29.
    Example 112. 2 -Bromo-4 - (methylsulfonyl) -1,2,2,3,3,4,4,5,5,6,6- undecafluorocyclohexanecarboxanilide, m.p. 150-152 ° C, yield 20%.
    Calculated,%: C 30.13; H 1.26; N 2.51.
    C (, N03.
    Found,%: C 30.04; H 1.32; N 2.50.
    Example 113. 2-Chloro 5 - (fluoro sulfonyl) -1,2,2., 3,3,4,4,5,5,6,6-un-decafluorocyclohexanecarboxanilide, mp 107 108 ° C, yield thirty%.
    Calculated,%: C 30.17; H 1.14; N 2.71.
    ,
    Found,%: C 30.16; H 1.01; N 2.78.
    Example 114. N- (2-BpoMo-4 nitro-1-naphthyl) -1,2,2,3,3,4,4,5,5,6, 6-undecafluorocyclohexanecarboxanilide, m.p. 152-1549C, yield 20%.
    Calculated,%: C 35.50; H 1.05; N 4.87.
    С, Н6ВгР „N, 0.
    Found,%: C 35.26; H 1.06; N 4.76.
    and-
    156182222
    Example 115. M- (4-Nitro 1-nafgtil) -1,2,2,3,3,4,4,5,5,6,6-undecafluoro-cyclohexanecarboxanilide, m.p. 155-156 ° C, yield 28%.
    Calculated,%: C 41.15; H 1.42; N 5.56.
    0
    five
    0
    five
    0
    five
    0
    five
    0
    five
    ,
    Found,%: C 40.99; H 1.21; N 5, 58.
    Example 116. 21 -Bromo-4 -nitro-b -cyano-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, m.p. 144-145 ° C, yield 13%.
    - Calculated,% i С 30,57; H 0.55; N 7.64.
    C14H3BrF.
    Found, 30.65; H 0.76; N 7.43.f
    Example 117. 2 -Bromo-4 -carbomethoxy-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, m.p. 128 - 131 C, yield 17%.
    Calculated,%: C 33.49; H 1.31; N 2, b.
    C, 5H7BrF41 N03.
    Found,%: C 33.49; H 1.41; N 2.90.
    Example 118. 2-Methyl-3-nitro 1,2,2,3,3,4,4,5,5,5,6,6-undecafluorocyclohexanecarboxanilide, so pl. 109-110 ° C, yield 43%.
    . Calculated,%: C, 36.54; H 1.53; N 6.09.
    C 4H7F41 N203.
    Found,%: C 36.25; H 1.75; N 5.99.
    EXAMPLE 119. 2 -Bromo-4-chloro-6-cyano-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, t.p. 113 - 115 ° C, yield 6%.
    Calculated,%: C 31.17; H 0.56; N 5.19.
    C14H3BrClF 4 N20.
    Found,%: C 31.28; H 0.63; N 5.31.
    Example 120. 2-Chloro-4-nitro b-cyano-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, mp. 145-147 ° C, yield 18%.
    Calculated,%: C 33.26; H 0.60; N 8.31.
    CI (VH, CIF, N2o ,.
    Found,%: C 33.27; H 0.77; N 8.08.
    PRI me R 121. 2 -Bromo-4-cyano-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, mp. 140-. 143 ° C, yield 40%.
    Calculated,%: C, 33.29; 1 0.80; N 5.55.
    CHH4Brl w.
    Found,%: C 33.49; H 0.83; N 5.26.
    Example 122. 2,4-Dichlorob-cyano-1,2,2,3,3,4,4,5,5,5,6,6-unde cafluorocyclohexanecarboxanilide, m.p. 90-93 ° C, yield 4, one%.
    Calculated,%: C, 33.97; H 0.61; N 5.66.
    С4 (Н3С1гР „N40.
    Found,%: C 34.04; H 0.66; N 5.42. (
    Example 123 2-Bromo-4 - (tr fluoromethyl) -1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, mp. 79-80 ° C, yield 19%.
    Calculated,%: C 30.68; H 0.74; N 2.56.
    Cj +.
    Found,%: C 30.73; H 0.88; N 2.43.
    EXAMPLE 124. 2, 6-Dichloro-, 2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, m.p. 166 ° C, yield 65%.
    Calculated,%: C, 26.20; H 0.51; N 2.35.
    With "1CS14R" NU.
    Found,%: C 26.54; L 0,00; N 2.30.
    II p im 125. 2, b - Dichloro-4G (toiitomethyl) -1.2,2,3,3,4,4,5, 6,6-undecafluorocyclohexanecarboxanide, so pl. 175-176 ° C, yield 40%.
    Calculated,%: C, 31.25; H 0.56; N 2.60.
    C (jH3ClzFHNO.
    Found,%: C 31.54; H 0.83; N 2.59.
    Example 126. 2 j3-dinitro 1,2,2,3,3,4,4,5,5,6,6-undecafluoride-lehexanecarboxanilide, i.e. 146-147 ° C, yield 11%.
     Calculated,%: C, 31.79; H 0.82; N 8.55.
    With „Н4Р„ Ig03.
    Found,%: C 31.93; H 0.82; N 8.68.
    Example of tyl-1,2,2,3,3,4,4,5,5,6,6-undecafta cyclohexanecarboxanilide, so pl. 85 86 ° C, yield 20%.
    Calculated,%: C 36.62; H 1.32; N 6.10.
    NbGpNgO ,.
    127. 2 Nitro-5 th
    Found 36.46; H 1.35; N 6.13.
    Example 128. 2, 4 -Dinitro-57- (methylthio) -1,2,2,3,3,4,4,5,5,6,6-un-decafluorocyclohexanecarboxanilide,
    Sodium (0.2 g, 0.008 mol) is added to 25 ml of ethanol. Methanethiol (0.5 g, 0.008 mol) is then bubbled into the solution, after which the compound of Example 55 2, 4-dinitro-5-fluoro-1,2,2,3,3,4,4 is added with stirring. , 5,5,6,6-undecafluorciclohexanecarboxanilide (2.0 g,
    from 0.004 mole). The reaction mixture is stirred at room temperature for more than 2 days. Then the reaction mixture is treated with HC1 / ice. The product precipitates and is discharged.
    0. Filtration is done, dried on
    air and recrystallized from toluene, So pl. 166-168 ° C, yield 51%.
    Calculated,%: C 31.30; And 1.13; N 7.82.
    5 Cf4H6F ,, Xo.
    Found,%: C 31.58; H 1.24; N 8.08.
    Example 129. 2,4-Dinitro-5-ethoxy-1,2,2,3,3,4,4,5,5,6,6-unQ decafluorocyclohexanecarboxanilide.
    The compound is obtained by reacting the compound of Example 55 of 2, 4-dinitro-5-fluoro-1,2,2,3,3,4,4,5,5,6,6-undec-fluorocyclohexanecarboxanilide with sodium ethyl acetate. The reaction and the treatment are carried out as described in Example 128. The product is initially melted at 73-85 ° C, recrystallized from ethanol and then melted
    0 at 105 ° C, yield 32%.
    Calculated,%: C 34.70; H 1.55; N 8.09.
    VH8F Kz ° 5Found,%: C 34.51; H 1.50; 5 N.
    Primer p 130. 2,6 -Dinitro-4 - bromo-1,2,2,3,3,4,4,5,5,6,6-undec-fluorocyclohex ank ar side with anilide, m.p. . 130-132 ° C, yield 7%.
    five
    Calculated,%: C 27.36; H Q, 53; N 7.36.
    C ,, H3BrFHN, 05.
    Found,%: C 27.68; H 0.78; N 7.21.
    EXAMPLE 131. 2, 6-Dichloro-4 / - cyano-1,2,2,3,3,4,4,5,5,6,6-undec-fluorocyclohexanecarboxanilide, mp. 220-221 ° C, yield 41%.
    Calculated,%: C, 33.97; H 0..61; N 5, b.
    CnHjClzF N20.
    Found,%: C 34.21; H 0.81; N 5.86.
    Example 132. 21 -Nitro-5-chloro-, 2,2,3,3,4,4,5,5,5,6,6-undecafluoro-cyclohexanecarboxanilide, m.p. 123-124 ° C, yield 35%.
    Calculated,%: C 32.49; H 0.84; N 5.83.
    C13H C- „Ng05,
    Found,%: C 32.29; H 0.91; N 5.88.
    Example 133. 2, 6-Dichloro-4-bromo-1,2,2,3,3,4,4,5,5,6,6 undecafluorocyclohexanecarboxanilide, mp 169-170 ° C, yield 50% .
    Calculated,%: C, 28.44; H 0955; N 2.55.
    ,, NO.
    Found,%: C 28.70; H 0.72; N 2.52.
    C, 7 H4F
    n
    ten
    15
    20
    Found,%: C 31.03; H 0.80; N 6.41.
    Example 138. 2 /, 4-Dinitrofluoro-1, 1,2,3,3,4,4,4a, 5,5,6,6,7,7, 8,8a-heptadecafluoro-1,2,3, 4.4a, 5.6, 8.8a-decahydro-2 naphthalenecarboxane lead, oil, yield 26%.
    Calculated,%: C 30.42; H 0.45; N 6.26.
    C17H ,, 0.
    Found,%: C 30.57; H 0.60; N 6.41.,
    L p i me R 139. 2 -Bromo-4-ni (trifluoromethyl) -1,2,2,3,4,4,5, 6,6-decafluorocyclohexanecarboxanil
    Approximately 130 cm3 of the anhydrous HF present in the pr are subjected to preliminary electrolysis in a teflon vessel equipped with a condenser and stainless steel maintained at a temperature of (-40) - (- 50) bc for the purpose of removing the last traces of water.
    Example 134
    about 2 cu. inches, consisting of alternating nickel plates and carbon steel plates in the atmosphere of nitrogen at a maximum current density of about 20 mA / cm2 and the voltage across the cell is equal to or lower than 5.2 V relative to the copper electrode compared to. 4.2 g (0.02 mol) of distilled m- (trifluoromethyl) benzoyl chloride are added and 5.6 A / h are passed (75% of the theoretical value. The reaction mixture is extracted with three portions of 20 cm3 of CPC1e and the extracts are added 3.2 g of 2-bromo-4-nitroaniline (0.015 mol) and 2.5 g (0.025 mol) of triethylamine in 25 cm3 of methylene chloride. The organic layer is washed with dilute hydrochloric acid, dried over sodium sulfate and separated using chromium chromatography on silica gel with toluene, 2-brpm-4-nitro 3- (trifluoromethyl) -1,2,2,3,4,4,5,5,6,6-deca fluorocyclohexanecarboxane is obtained id, mp 55-60 ° C, yield 35% from acid chloride (after recrystallization from toluene, mp 79-82 ° C), P19-NMR shows a mixture of cis and trans-isomers. An analogous procedure is used when each of the compounds of examples 140-143 and 145.
    bromo-1,2,2,3,3,4,4,5,5,6,6-undec-fluorocyclohexanecarboxanilide, m.p. 176-177 ° C, yield 37%.
    Calculated,%: C, 28.44; H 0.55; N 2.55.
    C 3H3BrCl2.F4, NO.
    Found,%: C 28.55; And 0.75; N 2.81.
    Example 135. 21.4-Dichloro-6, iodo-1,2,2,3,3,4,4,5,5,6,6 -undec-fluorocyclohexanecarboxanilide, m.p. 164-166 ° C, yield 33%.
    Calculated,%: C, 26.20; H 0.51; N 2.35.
    .
    Found,%: C 26.44; H 0.75; N 2.19.
    PRI me R 136. 2 Bromo-4 -nitro-1,1,2,3,3,4,4,4a, 5,5,6,6,7,7,8,8, 8a -heptadecafr-1,2,3,4,4a, 5,6,7,8, 8a-decahydro-2-naphthalenecarboxanilide m.p. 62-80 ° C, yield 34%.
    Calculated,%: C 29.72; H 0.59; N 4.08.
    Cl7H4BrF, 7 H40 3.
    Found,%: C 29.46; H 0.74; N 3.97.
    EXAMPLE 137. 2, 4-Dinitro-1, 1,2,3,3,4,4,4a, 5,5,6,6,7,7,8,8,8- heptadetaetor- 1,2,3, A, 4a, 5, b, 7,8,8-decahydro-2-naphthalenecarboxanilide, oil, yield 35%.
    Calculated,%: C, 31.26; H 0.62; N 6.43.
    C, 7 H4F
    n
    0
    five
    0
    Found,%: C 31.03; H 0.80; N 6.41.
    Example 138. 2 /, 4 -Dinitro5 fluoro-1,1,2,3,3,4,4,4a, 5,5,6,6,7,7,8, 8,8a-heptadecafluoro-1,2 , 3,4,4а, 5,6,7, 8,8а-decahydro-2 naphthalenecarboxanide, oil, yield 26%.
    Calculated,%: C 30.42; H 0.45; N 6.26.
    C17H ,, 0.
    Found,%: C 30.57; H 0.60; N 6.41.,
    Lrimer 139. 2 -Bromo-4 -nit- (trifluoromethyl) -1,2,2,3,4,4,5,5, - 6,6-decafluorocyclohexanecarboxanilide.
    Approximately 130 cm3 of commercially available anhydrous HF are subjected to preliminary electrolysis in a Teflon vessel equipped with a stainless steel condenser maintained at (-40) - (- 50) Bc for the purpose of removing the last traces of water.
    5 Use a block of electrodes volume
    0
    five
    0
    five
    0
    five
    about 2 cu. inches, consisting of interleaved nickel plates and carbon steel plates in a nitrogen atmosphere at a maximum current density of about 20 mA / cm2 and a cell voltage equal to or below 5.2 V relative to the copper reference electrode. 4.2 g (0.02 mol) of distilled m- (trifluoromethyl) benzoyl chloride are added and 5.6 A / h (75% of the theoretical value) are passed. The reaction mixture is extracted with three portions of 20 cm3 of CPC1e and the extracts are added to 3.2 g of 2-bromo-4-nitroaniline (0.015 mol) and 2.5 g (0.025 mol) of triethylamine in 25 cm3 of methylene chloride. The organic layer is washed with dilute hydrochloric acid, dried over sodium sulfate and separated using chromatography on silica gel with toluene. 2-Brpm-4-nitro 3- (trifluoromethyl) -1,2,2,3,4,4 is obtained. , 5,5,6,6-decafluorocyclohexanecarboxanilide, so pl. 55-60 ° C, yield 35% from the acid chloride (after recrystallization from toluene, mp. 79-82 ° C), P19-NMR shows a mixture of cis and trans-isomers. A similar procedure is used when obtaining each of the compounds in examples 140-143 and 145.
    Calculated,%: C 29.25; H 0.70; N 4.87.
    CMIUBrFn NaO}.
    Found,%: C 29.20; H 0.83; N 5.16.
    After recrystallization, it is found,% C 29.14; H 0.66; N 4.77.
    A 4% yield of the product, similar to the mixture of cis and trans isomers, was obtained using m-toluene chloride in the above reaction, by isolation of hydrofluoride from HF without the advantage of extraction.
    Found,%: C 29.36; H 0.80; N 4.79.
    Example 140, 2 -Bromo-4 -nitro-4- (trifluoromethoxy) -1,2,2,3,3,4,3, 5,6, b-where is caffluorocyclohexenecarboxanide, mp, 90-92 ° C, 20% yield from p (trifluoromethoxy) benzoyl chloride (as a result of hardly recrystallization from toluene, mp 101-104 ° C).
    Calculated,% t With 28,54; H 0.68; N 4.74,
    C, 4H4BrFrt H40E.
    Found,%: C 28.64; H 0.69; N 4.47.
    After recrystallization, C, 28.42; H 0.73; H 4.64. /,
    Example 141. 2f-Bromo-4-nitro-4- (pentafluoroethoxy) -1,2,2,3,3,4, 5,5,6,6-decafluorocyclohexanecarboxanilide, m.p. 75-91 ° C, yield 5% of p-ethoxybenzoyl chloride. After recrystallization from with at
    Calculated,%: C 28.08; H 0.62; 4.37.
    %
    toluene product melts 128-133 ° C.
    N
    C 5H4BrF 5.Na03.
    %:
    Found after recrystallization, C 28.38; H 0.75; N 4.66.
    Example 142. A mixture of 50:50 2-bromo-4-nitro-4 chloro-1,2,2,3,3,4,5, 5,6,6-decafluorocyclohexanecarboxanilide and 2-bromo-4-nitro -1,2,2,3,3, 4,4,5,5,6,6-undecafluorocyclohexane-carboxanilide, so pl. C, yield 11% of p-chlorobenzoyl chloride.
    Found,%: C 28.83; H 0.74; N 5.17.
    .BrClF o xyo.
    Calculated,% s With 29.15; H 0.93; N 4.86 s
    II p imper 143. A mixture of two isomers 2-bromo-4-nitro-x, x-dichloro, x, x, x, x, x, x, x, x-non-fluoropolycyclohexancarboxanilide, -bromo-4 -nitrox chloro-x, x, x, x, x, x, x, x, x, x-decafluoro-cyclohexanecarboxanilide and 2 bromo-4 -nitro-1,2,2,3,3,4,4 , 5,5,6,6-undecafluorocyclohexanecarboxanilide, oil
    0
    five
    five
    0
    N
    N
    0
    in relation to 22: 33, / e: 33., / 3: 11. Yield 6% from 2,4-dichlorobenzoyl chloride.
    Examples are p144. 2-4-Dinitro-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarboxanilide, dimethyl-bis (C 0 C 8) ammonium salt, oil, yield 92%.
    II p and mep 145, Mix 50:50 2 (- bromo-4g-nitro-2- (trifluoromethyl) -1,2, 3,3,4,4,5,5,6,6-decafluorocyclohexane-carboxanilide and 2-bromo-4-nitro, (trifluoromethyl) -x, x, x, x, x, x- 5 heptafluorcidopentanecarboxanilide, mp 66-8 () ° C, yield 5.1% of (trifluoromethyl) benzoyl chloride.
    Calculated,%: C, 29.24; H 0.70; 4, 87.
    С14Н4ВгН „ЫГО ,.
    Found,%: C 29.41; II 0.83; 4.67.
    Example 146. 2-Bromo-4-nitro-1, 2,2,3,3,4,4,5,5,5,6,6-undecafluoro-cyclohexanecarboxanilide.
    The compound, which is also described in Example 1, is prepared using another procedure, using p-nitroaniline as the starting material. 0 To a 100 ml round bottom flask equipped with a reflux condenser, stirrer, thermometer and addition funnel, add 37 ml of methylene chloride and 11.86 g of pyridine. Maintaining the contents of the reactor at 40 ° C using a water bath, 25.17 g of bromine is added over 3-5 minutes and the solution is stirred for 30 minutes at 20-25 ° C.
    50 ml of methylene chloride and 20.72 g of p-nitroaniline are placed in another 250 ml bottle equipped with a condenser, an additional funnel, a thermometer and a mechanical stirrer. 5 Maintaining the temperature below 30 ° C using a water bath, the solution of methylene chloride pyridine bromine obtained above was added dropwise to a suspension of p-nitroaniline in methylene chloride over 10 minutes. 20 ml of methylene chloride is additionally used to transfer the pyridine-bromine solution. The reaction mixture is stirred for 30 minutes at 25 ° C.
    The reaction mixture is then cooled in an ice bath to 0 ° C and 15.18 g of triethylamine are added in one portion. After that, over 15 minutes, 82.03 g of perfluorocyclohexanecarbonyl is added dropwise, keeping the temperature below 20 ° C, and the reaction mixture is stirred for 30 minutes at 5-1 ° C. Then, 100 ml of an aqueous solution of acetic acid (100 ml of water and 10 ml of acetic acid) are added to the reaction mixture and the reaction mixture is stirred for 10 minutes (pH 4.3). Then the layers are separated. The aqueous layer was extracted with three (40 ml) portions of methylene chloride. The layers of methylene chloride are mixed, washed with 110 ml of water and concentrated to an oily residue by distillation to 80 ° C (reactor temperature) 300 ml of methanol is added and 170 ml of mixed solvent are distilled off. While refluxing, 50 ml of water are added as quickly as possible. After that, the residue is slowly cooled to 0 ° C by stirring. The product precipitates and is removed by filtration, washed with two (60 ml) portions of cold methanol water (3: 1 v / v) and dried. Yield 69.75 g (86.3%).
    Example 147. 2 -Nitro-4-thiocyanato-1,2,2,3,3,4,4,5,5-undecafluoro-cyclohexanecarboxanilide, m.p. 81-83 ° C.
    Example 148. 2, 5-Dichloro-4 - bromo-1,2,2,3,3,4,4,5,5,6,6-undec-fluorocyclohexanecarboxanilide, m.p. 102-104 ° C, yield 46% o
    The compounds crawled by the proposed method are low toxic, especially in comparison with other compounds used as soil insecticides, such as counters.
    The proposed compounds are useful as insecticides, especially for controlling the flea beetle larvae. In combating these larvae, the residual effect of the compound is very important. In practice, substances to control the beetle of a long-haired beet must be used during the planting of maize, and the appearance of larvae occurs some time after planting. Therefore, it is necessary that the agent for the control of this bug beetle has a residual effect, otherwise the larvae will not be destroyed.
    This requirement for a residual effect is even stricter in those infrequent spring periods,
    when larvae are delayed due to weather. The advantage is that the proposed compounds have a good residual effect. Comparison data on the residual efficacy of the proposed compounds and the three compounds used as agents for the control of the flea beetle, is presented in Table. one.
    As can be seen from the presented data, the proposed compounds are superior to the compounds of the prior art in that they retain their oat-activity for many weeks longer than the known substances. The proposed compound of Example 1 and the known compound 4-chloro 2-hydroxy-6-oxo-1-cyclohexane 1-carboxanilide were tested. The tests were carried out against four insect species: the southern marching worm (SAW), the spider double-mite mite (2SSM), the melon and gourd aphid (MA), and the southern long-sighted flea (SCRW). A composition containing the corresponding compound was applied to each of the listed insects on the plants or, in the case of the last insect, to its larvae in the soil. For the first three insects, the concentration of the test compounds was 1.56–200 ppm in the composition. For SCRW, the concentration of the test compound in the composition, when applied to the soil, was 0.09-12.0 Cho / million.
    Results in% destruction are shown in Table. 2
    In the same way, the proposed compounds were tested in different m against the first three insects at a concentration of 200 ppm. and against the fourth - 12 ppm (SCRW). The results are shown in table 3.
    Thus, the compounds according to the invention showed excellent insecticidal properties in comparison with the known compound.
    权利要求:
    Claims (1)
    [1]
    Invention Formula
    The method of producing carboxanilides of the general formula
    About I Rj-C -N-R2
    H
    where R, is perfluorodecahidronaphthyl, un-decafluorocyclohexyl, decafluorocyclohexyl;
    RЈ is phenyl substituted with a para-nitro group, or 2-4 independently selected 1C groups, where R9 is bromine or chlorine,
    or two independently selected groups R4 where R4 is iodine, nitro, cyano, trifluoromethyl,
    or two groups of R3 and R, one of which is methyl, chlorine or bromine, and the other is nitro, methylsulfonyl or fluorosulfonyl,
    or two groups, one of which is methyl and the other is nitro or fluorosulfonyl.
    or in three groups, two of which are nitro, trifluoromethyl or chlorine, and a third - bromine or two chlorine groups, and a third nitro,
    or two nitro groups at positions 2 and 4, and a third - C4-C4-alkoxy or C-C-alkylthio in position 3 or 5,
    or by three groups, one of which is methyl, and two groups independently selected from the series containing chlorine or nitro;
    or R is naphthyl substituted by two groups representing nitro or bromine;
    Example 1 to 0.56
    gypsum1.12
    Example 10.56
    on florex1,12
    Example 770.56
    on florex1,12
    Diphonat1,12
    Counter1.12
    Timet1,12
    Control

    or their ammonium salts, where ammonium has the formula
    Rs Rs Rs.
    where is rg. and R6 each independently
    alkyl, benzyl,
    moreover, the total number of carbon atoms in all groups of Rs and 11 b is from 12 to 60, characterized in that the haloacyl of the formula
    ABOUT
    II
    RI-C-HQI
    where R4 has the specified value, is subjected to interaction with aniline or 1-aminonaphthalene General formula
    te2te-112
    where Ra has the specified value, in a neutral organic solvent, followed by isolation of the target product or transfer it to the corresponding ammonium salt.
    Table 1
    70
    00
    90
    00
    90
    90
    00
    90
    40
    ABOUT
    100
    100
    90
    100
    100
    100
    thirty
    ten
    ABOUT
    ABOUT
    Known compound
    Table 2
    35
    1561822
    J6
    Continuation of table 3
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    KR960010789B1|1996-08-08|Herbicidally active phenoxy-alkane-carboxylic acid derivatives
    EP0197756A2|1986-10-15|Alkanoyl anilides
    US4257805A|1981-03-24|Herbicidal |-3-|phenyl)ureas
    AU609973B2|1991-05-09|3-cyano-4-phenyl-pyrrole derivatives
    EP0035768A2|1981-09-16|Oxime esters, process and product for their preparation, their use and compositions containing these oxime esters
    EP0238351A2|1987-09-23|Molluscicides
    EP0152129B1|1991-06-12|N-acyl amino acid derivatives, their preparation and their use as fungicides
    JP2566991B2|1996-12-25|α-Haloketone derivative, method for producing the same and herbicide containing the same as an active ingredient
    同族专利:
    公开号 | 公开日
    ZA862480B|1987-02-25|
    ES553704A0|1987-09-01|
    KR900006517B1|1990-09-03|
    CA1283918C|1991-05-07|
    PH24477A|1990-07-18|
    PL149721B1|1990-03-31|
    EP0201193B1|1990-10-24|
    EP0201193A2|1986-11-12|
    DE3675069D1|1990-11-29|
    DD248952A5|1987-08-26|
    PT82322A|1986-05-01|
    RO95059B|1988-08-17|
    CN1012576B|1991-05-08|
    PL267525A1|1988-03-03|
    EP0201193A3|1988-05-18|
    NZ215672A|1990-11-27|
    RO95059A|1988-08-15|
    MY101438A|1991-11-18|
    GR860894B|1986-07-29|
    AU588296B2|1989-09-14|
    CN86102271A|1986-12-03|
    IL78393D0|1986-07-31|
    DK154486A|1986-10-06|
    HUT42750A|1987-08-28|
    AU5552586A|1986-10-09|
    KR860007874A|1986-11-10|
    ES8707922A1|1987-09-01|
    BR8601566A|1986-12-09|
    JPS61236756A|1986-10-22|
    IL78393A|1990-12-23|
    PL149800B1|1990-03-31|
    PT82322B|1988-10-14|
    DK154486D0|1986-04-04|
    GT198600181A|1987-09-26|
    AT57681T|1990-11-15|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    DE3211987A1|1981-04-03|1982-10-21|CIBA-GEIGY AG, 4002 Basel|Cyclobutanedicarboxylic acid derivatives, their preparation and their use as fungicide|GB8607033D0|1986-03-21|1986-04-30|Lilly Industries Ltd|Molluscicides|
    US5756000A|1996-02-06|1998-05-26|Minnesota Mining And Manufacturing Company|Perfluorocarbonyl fluoride compositions and their use|
    JP4601759B2|2000-03-09|2010-12-22|石原薬品株式会社|Perfluorodecalyl group-containing peroxide, method for producing the same, and method for producing perfluorodecalyl group-containing compound|
    CN104447433A|2014-11-11|2015-03-25|常州大学|Method for synthesizing 3,5-dibromoparatoluensulfonyl chloride|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    US72021285A| true| 1985-04-05|1985-04-05|
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