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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704551Generated: November 1, 2026

Methanesulfonyl chloride → 1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonate

https://huagongshe.com/reaction/1704551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one hydrateHCID 20385584—
SolventPyridineHCID 1049—
Product1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonateHCID 86735360—

Reaction Steps

To a solution of 52.5 parts of 1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one hydrate in 200 parts of pyridine is added dropwise 63 parts of methanesulfonyl chloride. The mixture is stirred and cooled on the air for 2 hours. The pyridine is evaporated. To the residue is added 500 parts of water and the formed precipitate is filtered off. It is dissolved in 350 parts of trichloromethane. This solution is dried over magnesium sulfate and evaporated. The residue is crystallized from 40 parts of methylbenzene, yielding 25.5 parts of 1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonate; mp. 118°-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04126688
Source datasetuspto-grants-1978_11
ORD IDord-0e0e80ea29364513ad250513dfca2d4c
Source noteuspto-grants-1978_11