HRID1031507

反应详情

EQUATION

反应方程式

HRID 1031507 的结构方程式

PROCEDURE

实验过程

In 1,2-dimethoxyethane (10 ml) was dissolved diethylphosphonoacetic acid morpholide (210 mg), to which was added 90% potassium tert-butoxide (100 mg). To the mixture was added, after the tert-butoxy potassium was completely dissolved, 5-(4-chlorophenoxy)-2-(3,4-dimethoxybenzoyl)pyridine (240 mg). The mixture was stirred for one hour at room temperature and for 6 hours at 50° C. to 60° C. The reaction mixture was concentrated, and there was added water (30 ml), followed by extraction with ethyl acetate (70 ml×2). The extract solution was dried over anhydrous magnesium sulfate, and was subjected to filtration to remove the magnesium sulfate. The filtrate was concentrated and purified by means of a silica gel column chromatography (eluted with ethyl acetate) to obtain 4-[3-(5-(4-chlorophenoxy)-2-pyridyl)-3-(3,4-dimethoxyphenyl)acryloxy]morpholine (Compound No.88) (300 mg) as a resinous solid.

WORKUP

后处理

  1. additionTo the mixture was added
  2. concentrationThe reaction mixture was concentrated
  3. additionthere was added water (30 ml)
  4. extractionfollowed by extraction with ethyl acetate (70 ml×2)
  5. dry with materialThe extract solution was dried over anhydrous magnesium sulfate
  6. filtrationwas subjected to filtration
  7. customto remove the magnesium sulfate
  8. concentrationThe filtrate was concentrated
  9. custompurified by means of a silica gel column chromatography (eluted with ethyl acetate)