HRID2410936

反应详情

EQUATION

反应方程式

HRID 2410936 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-15 °C

PROCEDURE

实验过程

3-Fluoro-4-methoxy-phenol (21.32 g; 0.15 mol) prepared according to literature [Freedman, J.; Stewart, K. T.; J. Heterocycl. Chem. 1989, 26, 1547-1554] is dissolved in dry dichloromethane (300 mL). The well stirred reaction mixture is cooled to −15° C. (ice/salt). A solution of bromine (23.97 g; 0.15 mol) in dry dichloromethane (75 mL) is dropped into the reaction mixture. After complete addition stirring is continued for one hour. Water (150 mL) containing sodium sulfite (3.0 g) is added to the reaction mixture. Stirring is continued at ambient temperature for 30 min. The organic layer is separated, ished with water (100 mL) and dried over MgSO4 in the presence of decolorizing charcoal. After filtration the solvent is completely removed under reduced pressure. The residue is crystallized from tert-butylmethylether/hexane to yield the title compound as a colorless solid.

WORKUP

后处理

  1. customreaction mixture
  2. additionAfter complete addition
  3. stirringstirring
  4. additionis added to the reaction mixture
  5. stirringStirring
  6. waitis continued at ambient temperature for 30 min
  7. customThe organic layer is separated
  8. dry with materialdried over MgSO4 in the presence of decolorizing charcoal
  9. filtrationAfter filtration the solvent
  10. customis completely removed under reduced pressure
  11. customThe residue is crystallized from tert-butylmethylether/hexane