HRID7732

反应详情

EQUATION

反应方程式

HRID 7732 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

2-(3-Methoxy-4-methylphenyl)-1,3-benzoxazole (1.0 g, 4.1 mmol), carbon tetrachloride (18 mL), benzoyl peroxide (66 mg, 0.3 mmol) and N-bromosuccinimide (970 mg, 5.4 mmol) was heated to reflux conditions under argon and placed under a UV light. After 1 h, no starting material was observed by TLC. After cooling mixture to rt, filtered, washing with dichoromethane. After concentrating filtrate in vacuo, the resulting colorless solid was purified by flash chromatography, using a gradient elution of 1:4 EtOAc:hexanes to EtOAc. This afforded the desired intermediate, 2-[4-(bromomethyl)-3-methoxyphenyl]-1,3-benzoxazole, as a colorless solid.

WORKUP

后处理

  1. temperatureto reflux conditions under argon
  2. filtrationfiltered
  3. washwashing with dichoromethane
  4. concentrationAfter concentrating filtrate in vacuo
  5. customthe resulting colorless solid was purified by flash chromatography
  6. washa gradient elution of 1:4 EtOAc