HRID339732

反应详情

EQUATION

反应方程式

HRID 339732 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To the solution of benzyl 3-(tert-butyldimethylsilyloxy)propylcarbamate (5 g, 15.5 mmol) in tetrahydrofuran (20 ml), sodium hydride (1.24 g, 31 mmol, 60% in mineral oil) and iodomethane (3.86 ml, 62 mmol) were added slowly. The reaction temperature was warmed up to room temperature, and stirred for overnight. The reaction was completed quenched by water and organic material was extracted with ether. After evaporation of volatile material under reduced pressure, the residue was purified with silica gel column chromatography (EtOAC:Hx=1:10) to give title compound (4.9 g, 94%) as light yellow oil.

WORKUP

后处理

  1. customThe reaction was completed quenched by water and organic material
  2. extractionwas extracted with ether
  3. customAfter evaporation of volatile material under reduced pressure
  4. customthe residue was purified with silica gel column chromatography (EtOAC:Hx=1:10)