• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The invention relates to calkyl aromatic alcohols, in particular, to the preparations of cyclopropane derivatives; .2 YOH © -sn 3 where Y-CI; RI - Ci-Gi-alkyl which is used in the preparation of fungicides. The purpose of the invention is the discovery of new intermediates. Getting lead in two ways. By treatment with C-Ci-C4-alkyl-4- (4-chlorophenyl) -but-1-en-4-ol with compound f-ly CH2ZiZ2, where Zi and Z2, which may be the same and different, mean halogens, in the presence of zinc metal 2. Treatment of a halide-substituted benzaldehyde) with an organometallic compound f-ly RI - - CHaM, where RI.: g is C1-C4-alkyl; M is a metal, followed by the action on the resulting unsaturated alcohol in the presence of metallic zinc with the compound CHaZtZa, where Zi and 22, which may be the same or different, mean halogen atoms. 2 sec. and 1 zp f-ly.
    公开号:SU1718722A3
    申请号:SU884613194
    申请日:1988-12-09
    公开日:1992-03-07
    发明作者:Джелф Кроули Патрик；Джон Урч Кристофер；Энтони Вортингтон Пол
    申请人:Сандос Аг (Фирма)；
    IPC主号:
    专利说明:

    The invention relates to a method for producing new cyclopropane derivatives of the formula γ QH С> СН-0Н- <Г W where Y is chlorine, Ri is alkyl С1-С4,
    where Y is CI; Ri is Ci-Ci-alkyl which are used in the preparation of fungicides. The purpose of the invention is the identification of new intermediates. Getting lead in two ways. By treating 3-Ci C4-alkyl-4- (4-chlorophenyl) -but-1-en-4-ol with the compound CH2Z1Z2, where Zi and Z2, which may be the same and different, are halogens in the presence of zinc metal 2. By treating the reptilized benzaldehyde reagent with an organometallic compound, Ri — CH = CH — CHgM, where Ri is C1-C4 alkyl; M is a metal, with subsequent action on the resulting unsaturated alcohol in the presence of zinc metal by the compound f-ly CH2Z1Z2, where Zi and Z2, which may be the same or different, mean halogen atoms. 2 sec and 1 s.p.
    used as intermediates in the production of agricultural pesticides, in particular in the production of α-aryl-a-cyclopropylalkyl-1H-azolyl derivatives of ethanol, including imidazolyl and 1,2,4-triazole ethanols, which are used as fungicides.
    A known method for the preparation of these fungicides, which consists in using as one of the intermediate compounds a ketone of the formula
    1718722 AZ
    ABOUT
    C1 ~ O <L · (A), which in turn is obtained in four stages from 4-chlorobenzylamine with a yield of 39%.
    The aim of the invention is to obtain new derivatives of cyclopropane, used as intermediates for the synthesis of fungicidal a-aryl-cyclopropylalkyl-1 H-azolyl derivatives of ethanol through a ketone of formula (A) in a simpler way and with a higher yield.
    This goal is achieved by the present, based on a Simmons-Smith type reaction, a method for producing cyclopropane derivatives of the formula (I), namely that the compound of the formula γ OH <JtyCH-CH-CH = CH 2 (II) R <
    where Y and Ri have the indicated meanings, are treated in the presence of zinc metal with a compound of the formula
    CH2Z1Z2 (III) where Ζι and Z2 are the same or different halogen atoms.
    Preferably, the process is conducted in the presence of a catalytic amount of sodium dihydride bis (2-ethoxymethoxy) -aluminate.
    This goal is also achieved by the method of obtaining derivatives of β-cyclopropane of the formula (I). consisting in the fact that the compound of the formula
    where Y ~ chlorine, • treated with an organometallic compound of the general formula
    Ri-CH = CH-CH 2 M '(V) wherein R) is Cg-Cd alkyl; M-metal.
    to obtain the compounds of the following formula sn-sn-sn = sn 2
    R1 where Y and Ri have the indicated meanings, which is treated in the presence of zinc metal with a compound of the above formula
    CH2Z1Z2, where Ζι and Z2 are the same or different halogen atoms.
    Example!. Obtaining 1- (4-chlorophenyl) -
    2-cyclopropylpropan-1-ol,
    Crotyl chloride (154.7 g, 1.71 mol) in dry tetrahydrofuran (130 ml) is added to the magnesium chip at such a speed of 15 to ensure continuous boiling c. reflux condenser. After completion of the introduction of the solution, the mixture is heated under reflux for another 1 h, and then cooled to 0 ° C. Then, 4-chlorobenzaldehyde (120.0 g, 0.854 mol) dissolved in dry tetrahydrofuran (780 ml) was added to the reaction mixture 20 over 2 hours. After another 1 h, the solution was decanted from excess magnesium into a saturated aqueous solution of ammonium chloride and the magnesium was washed with diethyl ether. 2M hydrochloric acid was added to dissolve the precipitate, followed by extraction of the resulting mixture with diethyl ether.
    The combined extracts were washed with water, dried and evaporated in vacuo. After partial purification by chromatography (on SIO2 using a mixture of hexane-ethyl acetate as eluent), 3-methyl35-4- (4-chlorophenyl) -but-1-en-4-ol (118.45 g, about 64%) is obtained with a purity of about 90%).
    A mixture consisting of 3-methyl-4-14-chlorophenyl) -but-1-en-4-ol (63.68 g, about 292 mmol with a purity of about 90%), dib40 rummethane (45.5 ml, 648 mmol), zinc powder (84.75 g, 1.296 mol) and copper (I) chloride (12.83 g, 130 mmol) in dry diethyl ether (180 ml), are refluxed in a bath with ultrasonic vaz45 action for 3.5 hours. Then the mixture was filtered (through celite) and the filtrate was poured into 2M hydrochloric acid. The mixture was extracted with diethyl ether, and then the combined extracts were washed, subsequently with 50% water, with saturated aqueous bicarbonate solution sodium and water, dried and evaporated in vacuo. Chromatography (on SIO2, hexane-ethyl acetate as eluent in a ratio of 100: 055 to 80:20) gives 1- (4-chlorophenyl) -2-cyclo-propyl-propan-1-ol (44.72 g, 73%).
    Brown liquid, melting point 35 ° C, boiling point 120 ° C at
    0.05 mmHg
    Example 2. Obtaining 1- (4-chlorophenyl) -2-cyclopropylethanol.
    Allyl chloride (97.88 g, 2.28 mol) dry tetrahydrofuran (500 ml) is added to a suspension of magnesium shavings (60.08 g, 5 2.47 mol) in dry tetrahydrofur not (50 ml) at such a rate as to allow continuous reflux. The mixture was then refluxed for another hour. Then, 4-chlorobenzaldehyde (120 g, 854 mmol) dissolved in dry tetrahydrofuran (600 ml) was added dropwise, and the reaction mixture was refluxed for another 2 hours. After cooling to room temperature, the mixture was poured into water with ice, carefully acidified with 1M hydrochloric acid and extracted with diethyl ether. The combined extracts were washed with brine, dried and evaporated in vacuo with 20 yield of crude 4- (4-chlorophenyl) but-
    1-en-4-ol (169.4 g with a purity of about 92%, which is used without further purification.
    The crude 4- (4-chlorophenyl) but-1-en-25 4-ol obtained in the previous step (85.37 g, about 430 mmol, with a purity of about 92%), zinc powder (121.5 g, 1086 mol ), copper (I) chloride (18.69 g, 187 mmol) and dibromomethane (163.6 g, 936 mmol), 30 dissolved in dry diethyl ether (250 ml), are heated under reflux for 3 hours in a bath ultrasonic exposure, and then poured into 2M hydrochloric acid. The resulting mixture was extracted with diethyl ether, and the extract was washed with 2M hydrochloric acid and brine. Then dried and evaporated in vacuo. After chromatography (SIO2): hexane ethyl acetate 90:10) 1- (4-chlorophenyl) - 40 is obtained
    2-cyclopropyl ethanol (37.24 g, 44% of 4 chlorobenzaldehyde).
    Example 3. Obtaining 1- (4-chlorophenyl) -2-cyclopropylpropan-T-ol using 45 dihydride bis- (2-methoxyethoxy) sodium aluminate (SDBA) as a catalyst.
    . * A suspension of 48 g (0.74 mol) of Zn and 0.5 g (0.005 mol) of copper chloride (1) in 88 g of toluene and 44 g of dimethoxyethane is prepared, and it is kept at 50 ° C. To the resulting suspension was added 1.8 g of a 70% solution of SDBA in acid. Then, 44 g (39.4 at 100% = 0.2 mol) are added to the resulting mixture.
    3- methyl-4- (4-chlorophenyl) but-1-en-4-ol. Within 55 hours, 101 g (0.58 mol) of dibromomethane were added at 95 ° C. After the introduction of dibromide methane was stopped, copper (I) chloride was added to the resulting mixture. To obtain the above compound, the reaction proceeds for 3 hours at 95 ° C. The product yield is 88.1%.
    Compounds of general formula (I) are used as intermediates 5 in the synthesis of fungicidal a-aryl-α-cyclopropylalkyl-1H-azolyl derivatives of ethanol via a ketone of formula (A).
    A ketone of formula (A) is obtained from a compound of formula (I) by oxidizing it using 10 a wide range of oxidizing agents, for example chromium trioxide in various solvents, pyridium chlorochromate and pyridinium dichromate, or the Moffat reaction (dimethyl sulfoxide, acetic anhydride and triethylamine), or one of its variations, especially Swern variation (dimethyl sulfoxide, oxalyl chloride and triethylamine).
    The following examples show the use of new compounds of formula (Ϊ) as intermediates for the synthesis of the ketone of formula (A) by Swern variation. t
    Example 4. Obtaining 1- (4-chlorophe25 nyl) -2gcyclopropylpropan-1-one.
    Oxalyl dichloride (22.2 ml, 255 mmol) is added to a mixed solution containing dimethyl sulfoxide (35 ml, 489 mmol) in dry dichloromethane (950 ml) at 30 -78 ° C under a nitrogen atmosphere. After 15 minutes, 1- (4-chlorophenyl) -2-cyclopropylpropan-1-ol (44.72 g, 212 mmol) dissolved in dry dichloromethane (330 ml) was introduced into the reaction solution for approximately 35 minutes. 35 After 75 minutes, triethylamine (154 ml, 1105 mmol) was added and the resulting mixture was warmed to room temperature. Hexane was then introduced and the resulting mixture was washed with 1M hydrochloric acid, saturated aqueous 40 sodium bicarbonate solution and water, dried and evaporated in vacuo. Chromatography (SiO2, ‘hexane-ethyl acetate (100: 0) - (90-10) gives 1- (4-chlorophenyl) -2 cyclopropylpropan-1-one (38.0 g, 86%).
    PRI me R 5. Obtaining 1- (4-chlorophyi nyl) -2-cyclopropylpropan-1-one.
    Oxalyl dichloride (5.5 ml, 63 mmol) is added dropwise to a stirred solution containing dimethyl sulfoxide 50 cid (5.5 ml, 78 mmol) in dry dichloromethane (150 ml), at -78 ° C. After 15 minutes, to the mixture 2 1- (4-chlorophenyl) -2cyclopropyl ethanol (5.00 g, 25.4 mmol) in dry dichloromethane (60 ml) was added. After 1 h, triethylamine (27.5 ml, 197 mmol) was added, followed by warming the mixture to room temperature and poured into water. The mixture was extracted with dichloromethane. the extracts are washed with water, dried and evaporated in vacuo to yield crude
    Ί going from 4-chlorobenzaldehyde in three stages with a yield of 48-50%, while in the known method, the ketone of formula (A) is obtained based on
    4-chlorobenzylamide in 4 steps in yield
    39%
    权利要求:
    Claims (3)
    [1]
    Claim
    1> Method for the preparation of cyclopropane derivatives of the general formula
    1- (4-chlorophenyl) -2-cyclopropylethanol, which is used further without further purification.
    The crude 1- (4-chlorophenyl) -2-cyclopropylethanone (from the previous reaction) dissolved in dry dimethylformamide (150 Ml) is added dropwise to a stirred suspension of sodium hydride purified with hexane '(4.57 g of a 60% dispersion in oil, 114 mmol) suspended in dry dimethylformamide (35 ml) in a nitrogen atmosphere. After 1 h, the reaction mixture was cooled to -30 ° C, and then iodomethane (16.2 g, 114 mol), dissolved in dry dimethylformamide (35 ml) was added very slowly. Then the mixture was poured into water, followed by extraction with diethyl ether. The extracts were washed with brine, dried and evaporated in vacuo. Chromatography (SIO 2 , hexane-ethyl acetate 95: 5) gives 1- (4-chlorophenyl) -2-cyclopropylpropan-1-one (7.66 g, about 70% purity, about 28% based on 1- (4 -chlorophenyl-2-cyclopropylethanol).
    Spectral analysis data.
    1- (4-Chlorophenyl) -2-cyclopropylpropan-1-one.
    IR (film), cm ’·: 3080: 2972: 2935; 1686; 1592; 1584; 1490; 1402; 1221; 1095; 1015: 977 and 844.
    # H NMR (CDCI3. 270 MHz): 7.86 (2H, m); 7.43 (2H, m); 2.74 (1H, q, J - 8.7 and 6.9 Hz); 1.28 (ZN, d, J = 6.69 Hz); 1.01 (1H, m); 0.54 (2H, m) and 0.18 (2H, m).
    m / v: 208 (15%); 141 (37); 139 (100); 111 (21); 75 (11); 69 (37) and 41 (16).
    3- Methyl-4- (4-chlorophenyl) -but-1-en-4-oia.
    IR spectrum (film), cm * 1 : 3430 (wide); 3083; 2980; 2883; 1642; 1600; * 1496; 1416: 1098; 1020; 924 and 828.
    * H NMR (СОС1з, 270 MHz): 7.40-7.15 (4Н, m); 5.76 (1H, m); 5.13 (2H. M); 4.61 and 4.13 (1H, 2 x d, J = 5.4 and 6.9 Hz); 2.55 and 2.42 (1H, q and p). J = 6.9 and 5.4 Hz and 6.9 Hz), 2.16 and 1.94 (1H, 2 x br s) and 0.98 and 0.87 (ZN, 2 x d, J = 6, 9 and 6.9 • Hz).
    m / o (chemical ionization, ammonia):
    [2]
    2- 13. (4%, Μ + 11Нз) and 196 (100%. M +).
    4- (4-Chlorophenyl) but-1-en-4-ol.
    ’H PMP (CDCl3, 270 MHz): 7.27 (4H, m); 5.76 (1H, ddt, J. = 15.4, 12.3 iB, 9 Hz); 5.12 (1.H, dd, J = 15.4, and 2 Hz); 5.11 (1H, doublet of doublets, J = 12.3 & 2 Hz); 4.67 (1H, t, J · 6.9 Hz); 2.89 (TH broad s) and 2.45 (2H, t, J = 6.9 Hz).
    Thus, using a compound of formula (I) as an intermediate. for the synthesis of fungicides, a ketone of formula (A) (which is then converted to a fungicide) is obtained from where Y is chlorine; Rt
    R.1 - Cd-Cd-alkyl. characterized in that the compound of the general formula
    OH ^^ sn-sn-sn = sn 2 where Υ and Ri have the indicated meanings, are treated in the presence of zinc metal with a compound of the general formula
    CH 2 ZiZ 2 , where Ζι and Z 2 , the same or different, are halogens.
    2. The method according to claim 1, characterized in that the process is conducted in the presence of a catalytic amount of dihydride-bis- (2ztoxy-methoxy) sodium aluminate.
    [3]
    3. A method of obtaining derivatives of cyclopropane of the General formula
    R, where Y is chlorine:
    Ri is Ct-Cd alkyl, characterized in that the compound of the general formula where Υ is chloro is treated with an organometallic compound of the general formula
    Ri — CH = CH — CH 2 M, where Ri is Ci-Cd alkyl;
    M is a metal to give a compound of the general formula
    I
    R1
    9 1718722 10 where Y and Ri have the indicated meanings, CH2Z1Z2.
    which is treated in the presence of meg · where Zi and Z2 are the same or different tallic zinc compounds of the formula. halogens.
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    引用文献:
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    DE3206225A1|1982-02-20|1983-09-01|Degussa Ag, 6000 Frankfurt|FUNGICIDELY EFFECTIVE BENZHYDROL DERIVATIVES|
    US4472313A|1982-09-20|1984-09-18|Sandoz, Inc.|Cyclopropanation of olefins|
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    CN105820128B|2015-01-05|2018-01-19|江西华士药业有限公司|A kind of preparation method of cyproconazole|
    CN105130772B|2015-07-29|2017-03-08|江苏七洲绿色化工股份有限公司|A kind of 1（4 chlorphenyls）The preparation method of 2 cyclopropyl 1 acetone|
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    GB878729107A|GB8729107D0|1987-12-14|1987-12-14|Chemical process|
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