HRID506447

反应详情

EQUATION

反应方程式

HRID 506447 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

Bis(2-methoxyethyl)aminosulfur trifluoride (4.5 g, 20.34 mmol) was added to a stirred solution of 1-(5-bromo-2-chlorophenyl)ethanol (3.99 g, 16.95 mmol) in dichloromethane (50 mL) at 0° C. The resulting solution was stirred at 0° C. for 3 h. The reaction mixture was quenched with a 5% solution of aqueous sodium bicarbonate (100 mL) and the resulting bubbling biphasic reaction mixture was vigorously stirred at 0° C. for 15 min. The reaction mixture was diluted with water (50 mL) and extracted with dichloromethane twice. The combined organic layers were washed with 1M hydrochloric acid, dried and concentrated by rotary evaporation. The product was purified by flash chromatography on silica gel (hexanes) to yield the title compound (2.65 g, 11.16 mmol, 65.8% yield) as a clear oil: 1H NMR (CDCl3) δ 7.65 (d, 1H), 7.37 (m, 1H), 7.20 (m, 1H), 5.88 (dq, 1H), 1.61 (dd, 3H).

WORKUP

后处理

  1. customThe reaction mixture was quenched with a 5% solution of aqueous sodium bicarbonate (100 mL)
  2. customthe resulting bubbling
  3. custombiphasic reaction mixture
  4. stirringwas vigorously stirred at 0° C. for 15 min
  5. extractionextracted with dichloromethane twice
  6. washThe combined organic layers were washed with 1M hydrochloric acid
  7. customdried
  8. concentrationconcentrated by rotary evaporation
  9. customThe product was purified by flash chromatography on silica gel (hexanes)