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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2H-Benzimidazol-2-one, 1,3-dihydro-6-chloro-1-phenyl- | HCID 108653 | — |
| Reactant | 3,4-Dimethoxybenzenesulfonyl chloride | HCID 2734183 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Chloro-1,3-dihydro-1-(3,4-dimethoxybenzenesulfonyl)-3-phenyl-2H-benzimidazol-2-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05585394 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-705fa175bcf64a5bb64f2447194325ca |
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| Source note | uspto-grants-1996_12 |
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