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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704546Generated: October 30, 2026

Methane → 6-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/1704546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantThionyl ChlorideHCID 24386—
Reactant6-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-oneHCID 20385651—
SolventChloroformHCID 6212—
Product6-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 2038558777.5%

Reaction Steps

To a stirred mixture of 22.6 parts of 6-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one and 300 parts of trichloromethane are added dropwise 32 parts of sulfinyl chloride. Upon completion, stirring is continued for 3 hours at reflux. After stirring with activated charcoal, the reaction mixture is filtered hot over hyflo. The filtrate is evaporated and the residue is dissolved in methylbenzene. The solution is washed a few times with water, dried, filtered and evaporated. The oily residue is triturated in 2,2'-oxybispropane. The solid product is filtered off and dried, yielding 19 parts (77.5%) of 6-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one; mp. 122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04126688
Source datasetuspto-grants-1978_11
ORD IDord-aa528d9060df47a7a9048a043d8d788b
Source noteuspto-grants-1978_11