反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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
- customFor the workup, the reaction mixture was evaporated at reduced pressure
- dissolutionthe residue dissolved in ethyl acetate (90 ml)
- extractionextracted with hydrochloric acid (2N, 90 ml)
- additionThe aqueous layer was treated with a solution of sodium hydroxide (2N, 100 ml) and solid sodium chloride
- additionwas added until saturation
- extractionThe following extraction with ethyl acetate (3×200 ml)
- customthe evaporation of the combined organic layers
- dry with materialafter drying over sodium sulphate