HRID274558

反应详情

EQUATION

反应方程式

HRID 274558 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

25 ml of tert.-butyllithium solution (1.4M in hexane) are added dropwise at -70° within 10 minutes to 10 g of 4-(benzyloxy)-3-methoxy-bromobenzene dissolved in 100 ml of tetrahydrofuran. After stirring at -70° for 1 hour, 5 g of quinoline-4-carbaldehyde dissolved in 50 ml of tetrahydrofuran are added dropwise within 30 minutes. The reaction mixture is stirred at -40° for 1 hour and at -5° for 1 hour, poured into 200 ml of water and adjusted to pH 4 with glacial acetic acid. The mixture is extracted three times with 50 ml of ether each time. The combined ether phases are washed with water, dried over sodium sulfate and evaporated. There is obtained α-[4-(benzyloxy)-3-methoxyphenyl]-4-quinolinemethanol as an amorphous solid.

WORKUP

后处理

  1. additionare added dropwise within 30 minutes
  2. stirringThe reaction mixture is stirred at -40° for 1 hour and at -5° for 1 hour
  3. extractionThe mixture is extracted three times with 50 ml of ether each time
  4. washThe combined ether phases are washed with water
  5. dry with materialdried over sodium sulfate
  6. customevaporated