HRID1639441

反应详情

EQUATION

反应方程式

HRID 1639441 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of 4.7 g of (S)α-cyano-3-phenoxy-benzyl (IR,cis) 2,2-dimethyl-3-(2-carboxyethynyl)-cyclopropane-carboxylate in 45 ml of ethyl acetate was hydrogenated in the presence of 500 mg of 10% palladium hydroxide on barium sulfate and 6.5 ml of quinoline and the mixture was filtered. The filtrate was washed with N hydrochloric acid, then with water until neutral, dried and evaporated to dryness. The 5.1 g of oil residue were chromatographed over silica gel and eluted with a 70-30-1 mixture of hexane-ethyl acetate-acetic acid to obtain 3.8 g of (S)α-cyano-3-phenoxy-benzyl (IR,cis) 2,2-dimethyl-3-[(Z) 3-hydroxy-3-oxo-1-propenyl]-cyclopropane-carboxylate.

WORKUP

后处理

  1. filtrationthe mixture was filtered
  2. washThe filtrate was washed with N hydrochloric acid
  3. dry with materialwith water until neutral, dried
  4. customevaporated to dryness
  5. customThe 5.1 g of oil residue were chromatographed over silica gel
  6. washeluted with a 70-30-1 mixture of hexane-ethyl acetate-acetic acid