HRID1416184

反应详情

EQUATION

反应方程式

HRID 1416184 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
40 °C

PROCEDURE

实验过程

6-(3-Hydroxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran (2.2 g) (see Preparation 9) was dissolved in dry dimethylformamide (4 ml) and imidazole (1.1 g) and tert-butyidimethylsilyl chloride (1.2 g) were added. The flask was fitted with a calcium chloride drying tube and the mixture was stirred at 40° C. for one hour. Water was added and the mixture was extracted with diethyl ether. The organic extract was washed with aqueous sodium hydrogen carbonate solution (×2), dried (anhydrous sodium sulphate), the solvent removed under reduced pressure and the crude product chromatographed on silica using (4:1 hexane: dichloromethane as the eluent to yield 6-(3-tert-butyldimethylsilyloxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran (2.84 g) as an oil.

WORKUP

后处理

  1. customThe flask was fitted with a calcium chloride drying tube
  2. extractionthe mixture was extracted with diethyl ether
  3. extractionThe organic extract
  4. washwas washed with aqueous sodium hydrogen carbonate solution (×2)
  5. dry with materialdried (anhydrous sodium sulphate)
  6. customthe solvent removed under reduced pressure
  7. customthe crude product chromatographed on silica using (4:1 hexane