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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258831Generated: November 2, 2026

Thionyl Chloride → HCID 21424806, compound

https://huagongshe.com/reaction/258831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 21424809HCID 21424809—
SolventChloroformHCID 6212—
ProductHCID 21424806HCID 2142480635.5%

Reaction Steps

To a stirred mixture of 13 parts of 6-chloro-1,3-dihydro-1-(2-hydroxyethyl)-2H-benzimidazol-2-one in 225 parts of trichloromethane are added dropwise 32 parts of sulfinyl chloride. Upon completion, stirring is continued for 7 hours at reflux temperature. The reaction mixture is evaporated and the residue is triturated in water. The solid product is filtered off and crystallized from a mixture of 2-propanol and 2,2'-oxybispropane. It is filtered off again and dried, yielding 5 parts (35.5%) of 6-chloro-1-(2-chloroethyl)-1,3-dihydro-2H-benzimidazol-2-one; mp. 164° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04035369
Source datasetuspto-grants-1977_07
ORD IDord-3bf032eb847349059ac19d55cc092832
Source noteuspto-grants-1977_07