HRID364628

反应详情

EQUATION

反应方程式

HRID 364628 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 27.6 g of ethyl 2,4-dichlorobenzoate and 20.81 g of ethyl 3-pyridylacetate at 20°-25° is treated portionwise with 10.59 g of sodium methoxide. The mixture is subsequently heated at 65°-70° and resulting readily volatile products are blown off with dry nitrogen. After 20 hours, the mixture is treated with 40 ml of concentrated hydrochloric acid and heated at reflux temperature for 18 hours. The mixture is washed with diethyl ether and the aqueous phase is made basic by adding concentrated ammonia and extracted with methylene chloride. The organic phase is concentrated and the crude product is chromatographed on silica gel with methylene chloride/methanol (98:2) to yield 2',4'-dichloro-2-(3-pyridyl)-acetophenone, which can be crystallized from diethyl ether/n-pentane and melts at 55°-56°.

WORKUP

后处理

  1. temperatureThe mixture is subsequently heated at 65°-70°
  2. customresulting readily volatile products
  3. temperatureheated
  4. temperatureat reflux temperature for 18 hours
  5. washThe mixture is washed with diethyl ether
  6. additionby adding concentrated ammonia
  7. extractionextracted with methylene chloride
  8. concentrationThe organic phase is concentrated
  9. customthe crude product is chromatographed on silica gel with methylene chloride/methanol (98:2)