HRID1449697

反应详情

EQUATION

反应方程式

HRID 1449697 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
120 °C

PROCEDURE

实验过程

A mixture of 2.11 g of 2-butyl-4-chloro-5-formyl-1-(2'-cyanobiphenyl-4-yl)methylimidazole, 8.38 g of trioctyltin azide (tri-n-octyltin azide) and 10 ml of toluene was stirred at 120° C. for 18 hours. After cooling, the reaction mixture was concentrated. To the residue was added 10 ml of ethanol as well as an aqueous solution of sodium nitrite (1.3 g/5 ml) and the mixture was adjusted to pH 3.3 with concentrated hydrochloric acid. The mixture was diluted with 20 ml of water and extracted with two 20 ml portions of ethyl acetate. The ethyl acetate solution was concentrated and the residue was purified by chromatography on 30 g of silica gel (CH2Cl2 -MeOH). The active fraction was concentrated to provide 1.82 g of 2-butyl-4-chloro-5-formyl-1-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methylimidazole. Yield 73%.

WORKUP

后处理

  1. temperatureAfter cooling
  2. concentrationthe reaction mixture was concentrated
  3. additionTo the residue was added 10 ml of ethanol as well as an aqueous solution of sodium nitrite (1.3 g/5 ml)
  4. additionThe mixture was diluted with 20 ml of water
  5. extractionextracted with two 20 ml portions of ethyl acetate
  6. concentrationThe ethyl acetate solution was concentrated
  7. customthe residue was purified by chromatography on 30 g of silica gel (CH2Cl2 -MeOH)
  8. concentrationThe active fraction was concentrated