HRID1859310

反应详情

EQUATION

反应方程式

HRID 1859310 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

2-(4-Methoxyphenyl)-3-(3-methoxyphenylthio)propionic acid obtained in Example 24 was dissolved in benzene (20 ml) and thionyl chloride (4.1 ml, 55.9 mmol) was added thereto. The reaction mixture was heated for 2 hours at 80° C. When the reaction is completed, the reaction solution was concentrated under reduced pressure to remove benzene and cooled to 5° C. Benzene (10 ml) was added to the reaction solution and then tin(IV) chloride (4.1 ml, 34.9 mmol) was slowly added dropwise thereto. The reaction mixture was stirred for 12 hours and then water (30 ml), concentrated hydrochloric acid (10 ml) and chloroform (30 ml) were added thereto. The reaction solution was heated under refluxing for one hour and extracted with chloroform. The organic layer was washed with water and sodium hydrogen carbonate solution, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified with column chromatography (n-hexane:ethyl acetate=8:2) to obtain 1 g (yield in two reaction steps: 20%) of the title compound as a yellow solid.

WORKUP

后处理

  1. concentrationthe reaction solution was concentrated under reduced pressure
  2. customto remove benzene
  3. temperaturecooled to 5° C
  4. additionBenzene (10 ml) was added to the reaction solution
  5. temperatureThe reaction solution was heated
  6. temperatureunder refluxing for one hour
  7. extractionextracted with chloroform
  8. washThe organic layer was washed with water and sodium hydrogen carbonate solution
  9. dry with materialdried over anhydrous magnesium sulfate
  10. concentrationconcentrated under reduced pressure
  11. customThe residue was purified with column chromatography (n-hexane:ethyl acetate=8:2)
  12. customto obtain