HRID1699561

反应详情

EQUATION

反应方程式

HRID 1699561 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

60 ml of a tetrahydrofuran solution of a Grignard reagent prepared from 2.4 g of 1-bromo-3,4-dimethoxybenzene was stirred with ice-cooling. Thereto was added 20 ml of a tetrahydrofuran solution of 3 g of 2-(3,4-diethoxyphenyl)-4-formylthiazole. The mixture was stirred at the same temperature for 1 hour and at room temperature for 3 hours. 10 ml of a saturated aqueous ammonium chloride solution was added. The solvent was removed by distillation. The residue was extracted with 100 ml of chloroform. The extract was washed with 20 ml of water and 20 ml of a saturated aqueous sodium chloride solution, and dried. The solvent was removed by distillation. The residue was purified by silica gel column chromatography (elutant: dichloromethane/acetone=99/1 by v/v) and recrystallized from diethyl ether to obtain 2.2 g of 2-(3,4-diethoxyphenyl)4-[1-hydroxy-1-(3, 4-dimethoxyphenyl)methlyl]thiazole.

WORKUP

后处理

  1. temperaturecooling
  2. stirringThe mixture was stirred at the same temperature for 1 hour and at room temperature for 3 hours
  3. customThe solvent was removed by distillation
  4. extractionThe residue was extracted with 100 ml of chloroform
  5. washThe extract was washed with 20 ml of water and 20 ml of a saturated aqueous sodium chloride solution
  6. customdried
  7. customThe solvent was removed by distillation
  8. customThe residue was purified by silica gel column chromatography (elutant: dichloromethane/acetone=99/1 by v/v)
  9. customrecrystallized from diethyl ether