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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448102Generated: November 1, 2026

Thionyl Chloride → HCID 20298704, compound

https://huagongshe.com/reaction/1448102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 20298711HCID 20298711—
SolventChloroformHCID 6212—
ProductHCID 20298704HCID 2029870485.8%

Reaction Steps

To a stirred mixture of 10.3 parts of α-[4-(diphenylmethyl)-1-piperazinylmethyl]-1-ethyl-2-methyl-1H-benzimidazole-5-methanol trihydrochloride in 75 parts of trichloromethane are added dropwise 4.3 parts of thionyl chloride at room temperature. Upon completion, stirring is continued for 30 minutes at reflux temperature After cooling, the precipitated product is filtered off, washed with trichloromethane and with 2,2'-oxybispropane, and dried, yielding 9 parts (85.8%) of 5-{1-chloro-2-[4-(diphenylmethyl)-1-piperazinyl]-ethyl}1-ethyl-2-methyl-1H-benzimidazole trihydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179505
Source datasetuspto-grants-1979_12
ORD IDord-1a48c47c40174cd9b14c0a70b571489a
Source noteuspto-grants-1979_12