HRID1731176

反应详情

EQUATION

反应方程式

HRID 1731176 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
10 °C

PROCEDURE

实验过程

2.7 ml of water and 1.4 ml of 12.5N potassium hydroxide were added to a solution of 2.7 g of ethyl 4-(m-benzoylphenyl)-3-hydroxy-butyrate in 27 ml of ethanol and the mixture was refluxed for 11/2 hours and then evaporated to dryness. The residue as taken up in 27 ml of water and the solution was treated with activated carbon, filtered and acidified to a pH of 1 by adding 10 ml of 2N hydrochloric acid with stirring at 10° C. The mixture was extracted with methylene chloride and the organic phase was washed with water, dried over sodium sulfate, treated with activated carbon, filtered and evaporated to dryness to obtain 2.36 g of 4-(m-benzoyl-phenyl)-3-hydroxy-butyric acid in the form of a colorless amorphous solid soluble in chloroform and insoluble in water.

WORKUP

后处理

  1. temperaturethe mixture was refluxed for 11/2 hours
  2. customevaporated to dryness
  3. additionthe solution was treated with activated carbon
  4. filtrationfiltered
  5. additionby adding 10 ml of 2N hydrochloric acid
  6. extractionThe mixture was extracted with methylene chloride
  7. washthe organic phase was washed with water
  8. dry with materialdried over sodium sulfate
  9. additiontreated with activated carbon
  10. filtrationfiltered
  11. customevaporated to dryness