HRID369688

反应详情

EQUATION

反应方程式

HRID 369688 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

First, 1.81 g of 3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(2,2-diethoxyethoxy)butyloxy)benzene was added to a mixture of 10 ml of acetic acid and 1 ml of concentrated hydrochloric acid with stirring under ice cooling. After further stirring for 15 minutes, the reaction mixture was poured into water and extracted twice with diethyl ether. The diethyl ether layers were combined and washed with water, aqueous sodium hydrogencarbonate solution and then saturated sodium chloride solution. The combined diethyl ether layer was dried over magnesium sulfate, and the diethyl ether was distilled out, which afforded 1.51 g of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetaldehyde (yield, 94%).

WORKUP

后处理

  1. stirringAfter further stirring for 15 minutes
  2. extractionextracted twice with diethyl ether
  3. washwashed with water, aqueous sodium hydrogencarbonate solution
  4. dry with materialThe combined diethyl ether layer was dried over magnesium sulfate
  5. distillationthe diethyl ether was distilled out