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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081492Generated: October 25, 2026

Water → 5-Chloro-1,3-dihydro-1-(3,4-dimethoxybenzenesulfonyl)-3-phenyl-2H-benzimidazol-2-one

https://huagongshe.com/reaction/1081492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2H-Benzimidazol-2-one, 1,3-dihydro-6-chloro-1-phenyl-HCID 108653—
Reactant3,4-Dimethoxybenzenesulfonyl chlorideHCID 2734183—
SolventDimethylformamideHCID 6228—
Product5-Chloro-1,3-dihydro-1-(3,4-dimethoxybenzenesulfonyl)-3-phenyl-2H-benzimidazol-2-oneHCID 15231540—

Reaction Steps

66 mg of sodium hydride as an 80% dispersion in oil were added in portions to a solution of 490 mg of 5-chloro-1,3-dihydro-3-phenyl-2H-benzimidazol-2-one in 5 ml of DMF and the reaction medium was stirred for 30 minutes. 520 mg of 3,4-dimethoxybenzenesulfonyl chloride were then introduced and the reaction medium was stirred overnight at room temperature. The solvent was then evaporated off under vacuum and the residue obtained was taken up with water. It was then extracted with DCM, washed with water and then dried over sodium sulfate and the solvent was evaporated off to dryness. The residue obtained was chromatographed on silica using a DCM/AcOEt mixture (95/5; v/v) as the eluent to give the expected product in the form of a white solid, which crystallized from absolute EtOH. m=0.71 g. M.p.=154° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05585394
Source datasetuspto-grants-1996_12
ORD IDord-705fa175bcf64a5bb64f2447194325ca
Source noteuspto-grants-1996_12