HRID1161020

反应详情

EQUATION

反应方程式

HRID 1161020 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

A solution of 2-fluoro-3-methoxy-phenol (0.5 g, 3.53 mmol) and dichloromethane is stirred at −78° C. A 1M solution of boron tribromide in dichloromethane (3.9 mL, 3.9 mmol) is added slowly and the mixture is stirred 10 min cold, then warmed to 0° C. and stirred 1 hr. The reaction is quenched with ice and stirred at room temperature overnight. The product is extracted with ethyl acetate (2×50 mL), dried over magnesium sulfate, filtered, and concentrated. The resulting residue is combined with boron trifluoride diethyl etherate (1.3 mL, 10.3 mmol) and acetic acid (0.2 mL, 3.28 mmol) and heated to reflux 8 hr. The mixture is cooled to room temperature, diluted with water (50 mL), and extracted with ethyl acetate (3×50 mL). The combined extracts are dried over magnesium sulfate, filtered and concentrated to about 10 mL volume. The resulting mixture is diluted with hexanes (50 mL), cooled to 0° C., and filtered to give the title compound (310 mg, 58%) as a tan solid. MS ES 171 M+1.

WORKUP

后处理

  1. stirringstirred 1 hr
  2. customThe reaction is quenched with ice
  3. stirringstirred at room temperature overnight
  4. extractionThe product is extracted with ethyl acetate (2×50 mL)
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. temperatureheated
  9. temperatureto reflux 8 hr
  10. temperatureThe mixture is cooled to room temperature
  11. extractionextracted with ethyl acetate (3×50 mL)
  12. dry with materialThe combined extracts are dried over magnesium sulfate
  13. filtrationfiltered
  14. concentrationconcentrated to about 10 mL volume
  15. additionThe resulting mixture is diluted with hexanes (50 mL)
  16. temperaturecooled to 0° C.
  17. filtrationfiltered