HRID704773

反应详情

EQUATION

反应方程式

HRID 704773 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of trans-4-amino-3,4-dihydro-2,2-dimethyl-3-hydroxy-2H-1-benzopyran-6-carbonitrile (193 g) and (-)-di-p-toluoyl-L-tartaric acid monohydrate (358 g) was dissolved in ethanol (600 ml) under reflux. The mixture was cooled to room temperature and stood for 3 days to give a white precipitate. This precipitate was collected by filtration, washed with a small volume of ethanol, and recrystallized twice from ethanol to give (-)-di-p-toluoyl-L-tartaric acid salt of (3S,4R)-4-amino-3,4-dihydro-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-6-carbonitrile (43.1 g).

WORKUP

后处理

  1. temperatureunder reflux
  2. customto give a white precipitate
  3. filtrationThis precipitate was collected by filtration
  4. washwashed with a small volume of ethanol
  5. customrecrystallized twice from ethanol