HRID399326

反应详情

EQUATION

反应方程式

HRID 399326 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a solution of 2,6-di-tert-butylphenol (2.06 g, 10 mmol) in EDC (50 mL) in a 200-mL round bottom flask, was added the stabilized BrCl brominating reagent (12 mL, about 11 mmol) dropwise, with stirring at room temperature. Initially, the orange reddish color of the reagent disappeared quickly. The color from the last 1 mL persisted for several minutes. The reaction mixture was allowed to stand for 30 minutes before being quenched with a few drops of sodium sulfite solution. After phase separation, it was diluted with EDC (50 mL), washed with water (100 mL) and dried (Na2SO4). The organic layer was concentrated under reduced pressure to afford a glue-like material. The material was redissolved in ether (10 mL) and after solvent removal, a crystalline solid 4-bromo-2,6-di-tert-butylphenol product (2.63 g, 92% recovered yield) was obtained in high purity (>98% by GC).

WORKUP

后处理

  1. waitThe color from the last 1 mL persisted for several minutes
  2. custombefore being quenched with a few drops of sodium sulfite solution
  3. customAfter phase separation, it
  4. additionwas diluted with EDC (50 mL)
  5. washwashed with water (100 mL)
  6. dry with materialdried (Na2SO4)
  7. concentrationThe organic layer was concentrated under reduced pressure
  8. customto afford a glue-like material
  9. customafter solvent removal