HRID420551

反应详情

EQUATION

反应方程式

HRID 420551 的结构方程式

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

  1. temperatureAfter cooling
  2. customthe solvent was evaporated under reduced pressure
  3. additionTo the residue was added water and 2N-aqueous hydrochloric acid
  4. extractionextracted with ethyl acetate
  5. washThe organic layer was washed with brine
  6. dry with materialdried over anhydrous sodium sulphate
  7. customevaporated under reduced pressure
  8. additionTo the residue, were added concentrated hydrochloric acid (0.65 ml) and ethanol (15 ml)
  9. stirringThe mixture was stirred at 80° C. for 8 hours
  10. temperatureAfter cooling
  11. customcondensed under reduced pressure
  12. customThe residue was purified by column chromatograph on silica gel (hexane:ethyl acetate=2:1)