HRID1978364

反应详情

EQUATION

反应方程式

HRID 1978364 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To 5.77 g (14.6 mM) of 1-[4-[N-(tert-butoxycarbonyl)aminomethyl]benzyl]-4-benzylpiperidine was added 10 ml (120 mM) of 12N-hydrochloric acid at room temperature and the mixture was stirred at the prevailing temperature for one hour. After addition of ethanol, the mixture was concentrated under reduced pressure and ethanol and diethyl ether were 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 white crystals.

WORKUP

后处理

  1. concentrationthe mixture was concentrated under reduced pressure and ethanol and diethyl ether
  2. additionwere added to the residue
  3. filtrationThe resulting crystal crop was harvested by filtration
  4. washrinsed with ethanol and diethyl ether