HRID4676

反应详情

EQUATION

反应方程式

HRID 4676 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 5-acetyl-6-methyl-4-(3-nitrophenyl)-2-phenylpyrimidine (3 g) and sodium borohydride (0.34 g) in methanol (110 ml) was stirred at room temperature for 4 hours. The reaction mixture was evaporated in vacuo and the residue was poured into a mixture of ethyl acetate and water. The separated organic layer was dried over magnesium sulfate and evaporated in vacuo. The crystalline residue was recrystallized from a mixture of n-hexane and diethyl ether to give a 5-(1-hydroxyethyl)-6-methyl-4-(3-nitrophenyl)-2-phenylpyrimidine (2.3 g).

WORKUP

后处理

  1. customThe reaction mixture was evaporated in vacuo
  2. additionthe residue was poured into a mixture of ethyl acetate and water
  3. dry with materialThe separated organic layer was dried over magnesium sulfate
  4. customevaporated in vacuo
  5. customThe crystalline residue was recrystallized from a mixture of n-hexane and diethyl ether