HRID635073

反应详情

EQUATION

反应方程式

HRID 635073 的结构方程式

PROCEDURE

实验过程

3-(S)-Tert-butyldimethylsilyloxy-4-(R)-(1-ethoxycarbonylcyclopropyl)-1-[1-(S)-phenylethyl]pyrrolidine (5.48 g, 13.15 mnmol) was dissolved in dry dichloroinethane (120 ml), and benzyl chloroformate (3.76 ml, 26.3 mmol) was added dropwise to the thus prepared solution which was cooled in an ice bath. After heating the reaction solution under reflux for 2 hours, dichloroinethane was evaporated under reduced pressure. Thereafter, the resulting residue was subjected to flash silica gel chromatography and eluted with an eluant of n-hexane:ethyl acetate=5:1, to thereby obtain 4.52 g (77%) of the title coinpound as a colorless oil.

WORKUP

后处理

  1. additionwas added dropwise to the thus prepared solution which
  2. temperaturewas cooled in an ice bath
  3. temperatureAfter heating the reaction solution
  4. temperatureunder reflux for 2 hours
  5. customdichloroinethane was evaporated under reduced pressure
  6. washeluted with an eluant of n-hexane
  7. customethyl acetate=5:1, to thereby obtain 4.52 g (77%) of the title coinpound as a colorless oil