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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178573Generated: October 29, 2026

Benzenesulfonyl chloride → HCID 67954034, compound

https://huagongshe.com/reaction/2178573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium hydrideHCID 24758—
ReactantHCID 67966902HCID 67966902—
SolventDimethylformamideHCID 6228—
ProductHCID 67954034HCID 67954034171.9%

Reaction Steps

To a solution of compound 15-B (0.563 g, 2.0 mmol) in DMF (13 mL) at 0° C. was added 60% NaH (0.096 g, 2.4 mmol) and the reaction mixture was stirred for 10 minutes. Benzenesulfonyl chloride (0.563 g, 2.4 mmol) was added and the reaction mixture was stirred at room temperature overnight. The reaction was quenched by the addition of H2O and the solution was extracted with ethyl acetate. After separation of the organic and aqueous layers a sufficient amount of water was added to remove any dissolved DMF from the organic layer. The organic layer was dried over Na2SO4, filtered, and the solvent evaporated under reduced pressure to afford the crude product. The crude material was purified by flash column chromatography, eluting with a hexanes-EtOAc gradient to give compound 15-C as a white solid (0.825 g, 86%); MS m/z (M+H+) 480.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067935B2
Source datasetuspto-grants-2015_06
ORD IDord-98837304391a46349c7930337bcdd3b2
Source noteuspto-grants-2015_06