HRID1978359

反应详情

EQUATION

反应方程式

HRID 1978359 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of 1.02 g (2.64 mM) of l-[trans-4-[N-(tert-butoxycarbonyl)aminomethyl]-1-cyclohexylmethyl]-4-phenylpiperidine in ethanol (10 ml) was added 10 ml (120 mM) of 12N-hydrochloric acid at room temperature and the mixture was stirred for one hour. This reaction mixture was concentrated under reduced pressure (crystals separated out) and diethyl ether was added to the residue. The resulting crystal crop was harvested by filtration and rinsed with ethanol and diethyl ether to provide the title compound as light-purple crystals.

WORKUP

后处理

  1. concentrationThis reaction mixture was concentrated under reduced pressure (crystals separated out) and diethyl ether
  2. additionwas added to the residue
  3. filtrationThe resulting crystal crop was harvested by filtration
  4. washrinsed with ethanol and diethyl ether