反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
CONDITIONS
反应条件
- 温度
- 80 °C
PROCEDURE
实验过程
To a mixture of [2-chloro-5-(methoxymethoxy)phenyl]acetonitrile (2.60 g; 12.3 mmol), sodium hydroxide (2.46 g; 61.5 mmol), water (10.4 ml) and ethanol (33.8 ml) was stirred at 80° C. for 3 hours. After cooling, the solvent was evaporated under reduced pressure. To the residue was added water and 2N-aqueous hydrochloric acid to become acid and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulphate, and evaporated under reduced pressure. To the residue, were added concentrated hydrochloric acid (0.65 ml) and ethanol (15 ml). The mixture was stirred at 80° C. for 8 hours. After cooling, the reaction solution was condensed under reduced pressure. The residue was purified by column chromatograph on silica gel (hexane:ethyl acetate=2:1) to give [2-chloro-5-hydroxyphenyl]ethyl acetate as colorless oil (0.69 g; 26%).
WORKUP
后处理
- temperatureAfter cooling
- customthe solvent was evaporated under reduced pressure
- additionTo the residue was added water and 2N-aqueous hydrochloric acid
- extractionextracted with ethyl acetate
- washThe organic layer was washed with brine
- dry with materialdried over anhydrous sodium sulphate
- customevaporated under reduced pressure
- additionTo the residue, were added concentrated hydrochloric acid (0.65 ml) and ethanol (15 ml)
- stirringThe mixture was stirred at 80° C. for 8 hours
- temperatureAfter cooling
- customcondensed under reduced pressure
- customThe residue was purified by column chromatograph on silica gel (hexane:ethyl acetate=2:1)