HRID1946911

反应详情

EQUATION

反应方程式

HRID 1946911 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

A solution of the (R)-4-(5-bromo-2-fluoro-phenyl)-4-methyl-oxazolidin-2-one (8.94 g, 33 mmol) in a 1:1-mixture of ethanol and water (120 ml) was treated with lithium hydroxide monohydrate (6.85 g, 163 mmol) and the reaction mixture was stirred at 100° C. overnight. For the workup, the reaction mixture was evaporated at reduced pressure and the residue dissolved in ethyl acetate (90 ml), then extracted with hydrochloric acid (2N, 90 ml). The aqueous layer was treated with a solution of sodium hydroxide (2N, 100 ml) and solid sodium chloride was added until saturation. The following extraction with ethyl acetate (3×200 ml) and the evaporation of the combined organic layers after drying over sodium sulphate yielded the (R)-2-amino-2-(5-bromo-2-fluoro-phenyl)-propan-1-ol as a white crystalline solid (7.90 g, 98% of theory, e.e.>98%).

WORKUP

后处理

  1. customFor the workup, the reaction mixture was evaporated at reduced pressure
  2. dissolutionthe residue dissolved in ethyl acetate (90 ml)
  3. extractionextracted with hydrochloric acid (2N, 90 ml)
  4. additionThe aqueous layer was treated with a solution of sodium hydroxide (2N, 100 ml) and solid sodium chloride
  5. additionwas added until saturation
  6. extractionThe following extraction with ethyl acetate (3×200 ml)
  7. customthe evaporation of the combined organic layers
  8. dry with materialafter drying over sodium sulphate