HRID1007074

反应详情

EQUATION

反应方程式

HRID 1007074 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

17 g of 4-[3-(3-bromo-3-phenylpropyl)-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]-benzonitrile are dissolved in 500 ml of dioxane and, after addition of 34 ml of ˜40 percent tetrabutylammonium trifluoroacetate solution, heated to reflux for 24 h. The mixture was concentrated to about half the volume, mixed with water and methyl tert-butyl ether and separated into the phases. The organic phase is concentrated, and the residue is stirred with 500 ml of ethanol and 200 ml of concentrated ammonia at room temp. for 1 h. It is then again concentrated in vacuo, and the crude product is purified on silica gel with dichloromethane/methanol =30:1 as mobile phase. The alcohol is obtained as an oil. MS (ESI): 413 (M+H+), 395 (M+H+-H2O) [C26H24N2O3 M=412].

WORKUP

后处理

  1. temperatureheated
  2. temperatureto reflux for 24 h
  3. concentrationThe mixture was concentrated to about half the volume
  4. additionmixed with water and methyl tert-butyl ether
  5. customseparated into the phases
  6. concentrationThe organic phase is concentrated
  7. concentrationIt is then again concentrated in vacuo
  8. customthe crude product is purified on silica gel with dichloromethane/methanol =30:1 as mobile phase