• 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:
    Chlorination of carbohydrates and alcohols utilizing a chlorinating reagent selected from triphenylphosphine oxide/ thionyl chloride, thiphenylphosphine oxide/phosgene, triphenylphosphine sulfide/thionyl chloride and triphenylphosphine sul- fide/phosgene.
    公开号:SU1634139A3
    申请号:SU864028402
    申请日:1986-10-20
    公开日:1991-03-07
    发明作者:А.Оъбрайен Элинор；Оъконнор Томас；Р.Дж.Тьюит Мэтью；Хай Лерой
    申请人:Макнейлэб, Инк. (Фирма)；
    IPC主号:
    专利说明:

    This invention relates to the chemistry of carbohydrate derivatives, and specifically to a process for the preparation of 1,6-dichloro-1,6-deoxy-ft-D-fructofuranosyl-4-chloro-4-deoxy-oi-D-galactopyranoside, which is a strong sweetening agent. having a sweetness several hundred times greater than sucrose
    The aim of the invention is to simplify the process for the preparation of 1,6-dichloro-1,6-dideoxy-13-fructofuranosyl-4-chloro-4-deoxy, -B-galactopyranoside.
    The goal is achieved by using a mixture of triphenylphosphine oxide with thionyl chloride or with phosgene or triphenylphosphyl sulfide with thionyl chloride as a chlorinating agent as a result of which the release of substances is reduced and the amount of impurities and by-products is reduced.
    Example 1 Sucrose (50 g, 0.14 mol) is mixed with N-methylmorpholine (60 g, 0.59 mol) in dimethylformamide (100 ml) at 50 ° C. Trityl chloride (141.8 g, 97% pure, 0.49 mol) is added in three portions in 2.5 hours and heating is continued for 3.5 hours. Sodium bicarbonate (42.7 g, 0.5 mol) is added and the mixture is heated at 50 ° C for 1 h. All solvents are removed in vacuo and the residue is dissolved in acetic anhydride (96.6 ml, 1.02 mol). Potassium acetate (15.6 g, 0.15 mol) is added and heated at 115 C for 3 hours. After cooling, methanol (400 ml) is added and after completion of the crystalO5 CO 4
    CO SO

    cm
    15
    solidification is obtained (183.2 g), which is 6,1,6-tri-0-trityl sugars pentaacetate (124,6 g, yield 68,8%) „
    Example 2 “Sucrose (40 g, 0.11 mol) is mixed with N-methylmorpholine (50 g, 0.49 mol) in dimethylformamide (120 ml) at 50 ° C. Trityl chloride (95 g, 97% - on a Q-qtot, 0.33 mol), dissolved in hot (60 ° C) toluene (60 ml), in three portions. Heating is continued for 3 hours, after which toluene (140 ml) is added. The mixture is extracted 50 ml portions of saturated sodium chloride solution at 60 ° C (to prevent the formation of emulsions) 0 After complete removal of N-methylmorpholine hydrochloride and dimethylformamide, a solution of 6,1,6 -tri-0-trityl sucrose in toluene is dried az after acetylation with acetic anhydride (75 ml, 0.8 mol) and pyridine (5 ml) at 90 ° C for 3 hours, followed by cooling and crystallization from methanol (420 ml) to form a solid (112.7 d) Content of the compound: 91.4% (103 g), which corresponds to 68.9% yield. Example 3c The compound (200 g) obtained in Example 2 is dissolved in toluene (800 ml) and the solution is cooled to 0 ° C, Hydrogen chloride gas (17.1 g) is passed into the cooled solution with stirring for about 4.5 hours, after which the suspension is stirred for e 15 min0 After vacuuming in the
    20
    25
    thirty
    five
    Q
    solid residue. The residue is suspended in methanol (120 ml) for 30 minutes, 6 ml of water is added and stirring is continued for another 10 minutes, Triphenylmethanol is filtered off (28.4 g) and washed with a solution of water (2 ml) in methanol (48 ml). The filtrate is evaporated to form an oil under reduced pressure and ethyl acetate (100 ml) is added to azeotropically remove any remaining water. The oil is dried overnight at 40 ° C under vacuum to obtain 26.4 g (58.2) of the product,
    Example 5, Compound (50 g) obtained in Example 3 was dissolved in water (100 ml) by heating to 60 ° C. The hot solution was filtered and cooled to room temperature. A base of pyridine row (collidin 2,4,6-trimethylpyridine) was added 2.5 ml and the resulting solution was stirred at room temperature for 2.5 hours. The solution was added with concentrated hydrochloric acid (2.5 ml) and er; strained with methylene chloride (2 x 125 ml). I The combined extracts are evaporated to 50 ml and heptane (50 ml) is added, the solution is stirred until crystallization occurs. The resulting suspension is diluted by adding heptane (2 x 50 ml) over 20 minutes and filtered. The crystals are washed with heptane (30 ml) and dried under vacuum at 45 ° C for 16 hours to obtain 2,3,6,3,4-pentaacetyl sucrose (34 g, 54%).
    PRI me R 6 "The compound (100 g) obtained in example 3 is heated
    0
    five
    0
    1 hour to remove traces of chlorine by boiling in methyl isobutyl ketone
    (500 ml) containing acetic acid (30 ml) for 3 h. The solution is cooled to room temperature, heptane (500 ml) is added, the resulting 2,3,6,3, 4-petaacetyl sucrose is filtered, washed with heptane (100 ml) and dried0 Yield 86 g (85%) 0
    hydrogen is purged with nitrogen. The mixture is filtered and washed with toluene (65 ml), crushed and suspended in toluene containing 1% triethylamine (120 ml) for 10 min. The mixture is again filtered, washed with toluene (65 ml), the precipitate is dried, receiving 87 g (80%) 2,3,4, h, 4; - penta-0-acetyl-sucrose;
    Example 40 Sucrose (50 g) is dissolved in 150 ml of methylene chloride, 15 ml of methanol containing 0.2 eq. Of hydrogen chloride (O $ 5 M) are added, the solution is stirred at room temperature for 4.5 hours. Hydrogen chloride is neutralized by tert- butylamine (1 ml). Methylene chloride and methanol are evaporated at room temperature under vacuum to obtain
    about when boiling in methyl isobutyl ketone
    (500 ml) containing acetic acid (30 ml) for 3 h. The solution is cooled to room temperature, heptane (500 ml) is added, the resulting 2,3,6,3,4-pentaacetyl sucrose is filtered, washed heptane (100 ml) and dried0 Yield 86 g (85%) 0
    Example 7 To a stirred at room temperature suspension of the compound (50 g) obtained in Example 5 and triphenylphosphine oxide (50.3 g) in toluene (150 g) were added thionyl chloride (32.8 ml). The resulting solution was boiled in for 2.5 hours, cooled to 40 ° C, water (200 ml) is added, the mixture is vigorously stirred at 0 ° C for 1 hour. The filter is rotary and washed with a mixture of toluene and all 5
    516
    dyes (1: 2.75 ml) o Get technical pentaacetate 4.1, b-trichloro-4.1, b trideoxygalactosucrose, which is recrystallized from hot methanol (200 ml), followed by stirring at -20 C for 1 h. 40 g (75%).
    Example To a suspension of 2,3,6, 3, 4-penta-0-acetyl sucrose (59 g, 90.4 mmol) and triphenylphosphine oxide (125.8 g, 454 mmol) in 1,2-dichloroethane add thionyl chloride (32.8 ml, 452 mmol) at room temperature and the mixture is heated at boiling for 3 hours. A solution of sodium bicarbonate (20 g) in 220 ml of water is slowly added, and the two-phase mixture is shaken for 5 hours. The organic layer is separated, evaporated dry under vacuum and add methyl isobutyl ketone (150 ml). While cooling to 0 ° C, triphenyphosphine oxide (98 g) is separated for 1 h, which is filtered off, washing the precipitate with water with methyl isobutyl ketone (50 ml) o The mother liquor is evaporated to dryness in vacuo and the residue is recrystallized from ethanol to give 4.1, 6-trichloro-4,1, 6-tristoxy-2,3,6,3, 4 -penta- 0-acetylgalactosaccharose (97.1 g), slightly contaminated with triphenylphosphine oxide
    Example 9 A phosgene (20 g, 0.202 mol) is passed through a suspension of triphenylphosphine oxide (45 g, 0.162 mol) in toluene at 45 ° C To the resulting mixture, after 30 minutes of shaking and subsequent degassing with nitrogen, add the compound (20 g, 0.0362 mol obtained in example 5, the resulting mixture was boiled (110-1 14 ° C) for 3 hours. After cooling to 0 ° C, 170 ml of water was added. After further cooling to 0 ° C for 1 hour, the mixture was filtered, obtaining 64.7 dry technical product. After crystallization from methanol, 4.1, 6 tons of trichloro-4,1,6g-trideoxy 2,3,6,3, 4 -penta-O-ac tilgalaktosaharozu (8.9 g).
    Example 10 To a suspension of the compound (50 g) obtained in Example 5 and triphenylphosphine sulfide (53.3 g) in xylene (150 ml) is added thionyl
    g 0 5 0
    Q 5 0
    five
    396
    chloride (32.8 ml), the mixture is heated at 4.5 hours, water (300 ml) is added. The two-phase system is stirred vigorously at 0 ° C for 1 hour. The technical product is isolated by filtration and recrystallized from methanol ( yield 31.8 g, 66%) 0
    权利要求:
    Claims (1)
    [1]
    Example 11. The compound (50 g) obtained in Example 7 was stirred at room temperature with sodium methylate in methanol (125 ml) for 1.5 hours under vacuum, it was dissolved for 10 minutes. The solution was neutralized with stirring Amberlite resin IRC 50 (H +) (7.5 g) 0 The resin is removed by filtration and washed with methanol (25 ml), the filtrate and washings are stirred to decolorize with activated carbon (2 g) and zeolite (2 g) for 15 min „The solution is purified by filtration and evaporated to a foam in vacuum. The residue is crystallized from ethyl acetate. (100 ml), filtered, washed with ethyl acetate (25 ml) and dried in vacuum at 40 ° C for 12 hours. Get 1,6-dichloro-1,6-dideoxy - $ - B-fructofuranosyl-4-chloro-4 - deoxy-f (-1) -galactopyranoside Yield 26 g, 92%. Claims of the invention
    A method for preparing 1,6-dichloro-1,6-dideoxy-B-1) fructofuranosyl-4-chloro-4-deoxy-p (-1) -galactopyranoside by reacting sucrose with trityl chloride, acetylating the tritylated derivative with acetic anhydride, detritating the resulting penta-acetate 6,1,6 -tri-0-trityl sucrose, followed by isomerization of the resulting 2,3,4,3,4-penta-0-acetyl sucrose, by chlorination of the resulting 2,3,6, 3, 4-penta- 0-acetyl saccharoids with the preparation of 4,1,6-trichloro-4,1, 6-grydesoxy-galactosucrose pentaacetate and its subsequent deacetylation, characterized in that About, in order to simplify the chlorination process, it is carried out using a mixture of triphenylphosphine oxide with thionyl chloride or with phosgene or triphenylphosphyl sulfide with titanium chloride.
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    同族专利:
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    GB858525954A|GB8525954D0|1985-10-21|1985-10-21|Chlorination of carbohydrates &c alcohols|
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