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
A mixture of 12.94 parts of ethyl (2-bromoethyl)carbamate, 15.68 parts of 5-chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one, 10.08 parts of sodium hydrogen carbonate and 160 parts of ethanol is stirred and refluxed overnight. The formed precipitate is filtered off and washed with trichloromethane. The layers from the filtrate are separated. The organic phase is dried, filtered and evaporated. The residue is stirred in 2-propanone. The unreacted starting material is filtered off and the filtrate is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from ethanol 70%. The product is filtered off and dried, yielding 6.5 parts of ethyl {2-[4-(5-chloro-2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]-ethyl}carbamate; mp. 187.7° C.
WORKUP
后处理
- temperaturerefluxed overnight
- filtrationThe formed precipitate is filtered off
- washwashed with trichloromethane
- customThe layers from the filtrate are separated
- customThe organic phase is dried
- filtrationfiltered
- customevaporated
- stirringThe residue is stirred in 2-propanone
- filtrationis filtered off
- customthe filtrate is purified by column-chromatography over silica gel using
- additiona mixture of trichloromethane and methanol (90:10 by volume) as eluent
- customThe pure fractions are collected
- customthe eluent is evaporated
- customThe residue is crystallized from ethanol 70%
- filtrationThe product is filtered off
- customdried