HRID269457

反应详情

EQUATION

反应方程式

HRID 269457 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

To a solution of 22.2 g (83.2 mmol) of 7-bromo-5-isopropyl-2-methyl-1-indanone in 120 ml of THF-methanol (2:1, vol.), 5.06 g (133 mmol) of NaBH4 was added, while vigorously stirring, over 3 h at 0° C. This mixture was stirred overnight at room temperature; then, 300 ml of cold water was added and the resulting mixture was acidified with 1 M HCl to pH 1. The organic layer was separated, and the aqueous layer was extracted with 3×150 ml of dichloromethane. The combined extract was dried over K2CO3 and evaporated to dryness, and 200 ml of toluene was added to the yellowish oil obtained. This toluene solution was treated with a catalytic amount of pTolSO3H (ca. 0.2 g) for 1 h at reflux, cooled to room temperature, and evaporated to dryness. The crude product was purified using flash chromatography on Silica Gel 60 (40-63 μm, d 40 mm, l 400 mm; eluent: hexanes). Yield 19.6 g (94%).

WORKUP

后处理

  1. stirringThis mixture was stirred overnight at room temperature
  2. customThe organic layer was separated
  3. extractionthe aqueous layer was extracted with 3×150 ml of dichloromethane
  4. extractionThe combined extract
  5. dry with materialwas dried over K2CO3
  6. customevaporated to dryness, and 200 ml of toluene
  7. additionwas added to the yellowish oil
  8. customobtained
  9. temperatureat reflux
  10. temperaturecooled to room temperature
  11. customevaporated to dryness
  12. customThe crude product was purified