HRID65391

反应详情

EQUATION

反应方程式

HRID 65391 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture consisting of 25.4 g of 4-(4-trifluoromethylphenoxy)phenol, 14.5 g of anhydrous potassium carbonate, 33.8 g of 2-(4-chlorobenzylthio)ethyl 2-bromopropionate and 150 ml of dry acetonitrile was refluxed for 3 hours with vigorous stirring. After cooling the reaction mixture to room temperature, the acetonitrile was removed under reduced pressure. Then, 150 ml of toluene were added to the residue and the resulting mixture was washed successively with 1% strength by weight aqueous sodium hydroxide solution and water, followed by dehydration. Upon distilling off the toluene under reduced pressure, there were obtained 46.4 g of 2-(4-chlorobenzylthio)-ethyl 2-[4-(4-trifluoromethylphenoxy)-phenoxy]-propionate in the form of a colorless oil.

WORKUP

后处理

  1. temperaturewas refluxed for 3 hours with vigorous stirring
  2. customthe acetonitrile was removed under reduced pressure
  3. additionThen, 150 ml of toluene were added to the residue
  4. washthe resulting mixture was washed successively with 1% strength by weight aqueous sodium hydroxide solution and water
  5. distillationUpon distilling off the toluene under reduced pressure