HRID1872485

反应详情

EQUATION

反应方程式

HRID 1872485 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
38 °C

PROCEDURE

实验过程

5 Millimolar potassium dihydrogen phosphate solution (50 ml) was adjusted to pH 7.1 with 0.1N sodium hydroxide solution (2 ml), porcine pancreatic lipase (Biocatalysts, Treforest, UK) (0.2 g) added and the pH again adjusted to 7.1 with 0.1N sodium hydroxide solution (2 ml). Racemic butyric ester derived from N-(4-benzoylphenyl)-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide (1 g) was dissolved in MTBE (10 ml) and added to the reaction, washing in with further MTBE (2 ml). The reaction was stirred at 38° C. under pH control initially set at 7.05 max/7.00 min. After 24 hr., further porcine pancreatic lipase (0.8 g) was added and the pH adjusted to 7.55 max/7.50 min and left for a further 42 hours when a total of 10 ml of 0.1 N sodium hydroxide had been added. The reaction mixture was acidified to pH 3.5 with 2 N HCl (2 ml), stirred for 15 min., then ethyl acetate (30 ml) was added and the mixture was stirred for a further 10 min. The mixture was then filtered and the residue washed with ethyl acetate (20 ml). The aqueous phase was separated and extracted with ethyl acetate (30 ml). The combined organic extracts were washed with 50% brine (20 ml), filtered and evaporated to an oil which partly crystallized. Yield: 0.95 g. The product was a mixture of the (R)-alcohol (99% enantiomeric excess) and ester.

WORKUP

后处理

  1. additionadded
  2. additionadded to the reaction
  3. washwashing in with further MTBE (2 ml)
  4. custominitially set at 7.05 max/7.00 min
  5. addition, further porcine pancreatic lipase (0.8 g) was added
  6. customadjusted to 7.55 max/7.50 min
  7. waitleft for a further 42 hours when a total of 10 ml of 0.1 N sodium hydroxide
  8. additionhad been added
  9. stirringstirred for 15 min.
  10. additionethyl acetate (30 ml) was added
  11. stirringthe mixture was stirred for a further 10 min
  12. filtrationThe mixture was then filtered
  13. washthe residue washed with ethyl acetate (20 ml)
  14. customThe aqueous phase was separated
  15. extractionextracted with ethyl acetate (30 ml)
  16. washThe combined organic extracts were washed with 50% brine (20 ml)
  17. filtrationfiltered
  18. customevaporated to an oil which
  19. custompartly crystallized
  20. additiona mixture of the (R)-alcohol (99% enantiomeric excess) and ester