HRID1281193

反应详情

EQUATION

反应方程式

HRID 1281193 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
20 °C

PROCEDURE

实验过程

A solution of N-tert-butoxycarbonyl-3(S)-amino-2(R)-hydroxy-4-phenylbutyric acid methyl ester 99 g dissolved in ethanol 130 ml was kept at 15-25° C. and mixed with sodium borohydride 15.7 g and stirred at 15-25° C. for 2.5 hrs. The reaction solution was diluted with water, adjusted with 6N-HCl to pH 2.5-3.5 and thereafter the solvent was distilled away to half the volume of the resultant solution, and then ethyl acetate was added to the solution. The solution thus obtained was washed with water and aqueous 10% sodium chloride solution successively to separate an organic phase. The solvent in the organic phase was distilled away and then ethyl acetate was added to the resultant concentrated solution to cool it and n-heptane was added to the solution halfway. Further n-heptane was added to the cloudy solution obtained. Thereafter, the solution was stirred at 10° C. to deposit crystals, which were filtered and dried in vacuum to obtain the N-tert-butoxycarbonyl-3(S)-amino-2(R)-hydroxy-4-phenyl-1-butanol(65.4 g).

WORKUP

后处理

  1. customwas kept at 15-25° C.
  2. distillationthe solvent was distilled away to half the volume of the resultant solution
  3. additionethyl acetate was added to the solution
  4. customThe solution thus obtained
  5. washwas washed with water and aqueous 10% sodium chloride solution successively
  6. customto separate an organic phase
  7. distillationThe solvent in the organic phase was distilled away
  8. additionethyl acetate was added to the resultant concentrated solution
  9. temperatureto cool it and n-heptane
  10. additionwas added to the solution halfway
  11. additionFurther n-heptane was added to the cloudy solution
  12. customobtained
  13. stirringThereafter, the solution was stirred at 10° C.
  14. filtrationwere filtered
  15. customdried in vacuum