HRID1978359
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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
- concentrationThis reaction mixture was concentrated under reduced pressure (crystals separated out) and diethyl ether
- additionwas added to the residue
- filtrationThe resulting crystal crop was harvested by filtration
- washrinsed with ethanol and diethyl ether