HRID461521

反应详情

EQUATION

反应方程式

HRID 461521 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
-70 °C

PROCEDURE

实验过程

A solution of 3-(m-phenoxyphenyl)-butyryl chloride (1 g.) (from the corresponding acid (1 g.) using excess oxalyl chloride in benzene) in ether (20 ml) was added dropwise to a solution of dimethyl copper lithium at -70° C under nitrogen (from methyl lithium (0.2 g.) and cuprous iodide (1 g.)) in ether (50 ml) and the mixture stirred a further 15 minutes at -70° C. Methanol was added to quench the reaction and the mixture was diluted with water, acidified and filtered through a pad of Kieselguhr. The ether layer was washed with sodium carbonate solution and with water, dried over anhydrous magnesium sulphate and evaporated to give a colourless oil. The product was purified by column chromatography to give 4-(m-phenoxyphenyl)-2-pentanone as a colourless oil.

WORKUP

后处理

  1. customto quench
  2. customthe reaction
  3. filtrationfiltered through a pad of Kieselguhr
  4. washThe ether layer was washed with sodium carbonate solution and with water
  5. dry with materialdried over anhydrous magnesium sulphate
  6. customevaporated
  7. customto give a colourless oil
  8. customThe product was purified by column chromatography