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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050265Generated: October 31, 2026

Thionyl Chloride → HCID 20506337, compound

https://huagongshe.com/reaction/2050265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 805032HCID 805032—
SolventChloroformHCID 6212—
ProductHCID 20506337HCID 20506337—

Reaction Steps

To a stirred and refluxing mixture of 7 parts of 2-ethyl-1H-benzimidazole-1-ethanol and 150 parts of trichloromethane are added dropwise 16 parts of sulfinyl chloride. Upon completion, the whole is heated to reflux and stirring is continued for 2 hours at reflux temperature. The reaction mixture is cooled and evaporated. Water is added to the residue and the whole is stirred with activated charcoal. The latter is filtered off and the filtrate is alkalized. The product is extracted with trichloromethane. The extract is dried, filtered and evaporated. The residue is crystallized from 2,2'-oxybispropane. The product is filtered off and dried, yielding 1-(2-chloroethyl)-2-ethyl-1H-benzimidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04200641
Source datasetuspto-grants-1980_04
ORD IDord-8b288db6ff9442289e3fd5968e068104
Source noteuspto-grants-1980_04