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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823109Generated: October 25, 2026

Benzamide → N-(4-bromobenzenesulfonyl)benzamide

https://huagongshe.com/reaction/1823109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzamideHCID 2331—
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-(4-bromobenzenesulfonyl)benzamideHCID 76616252.7%

Reaction Steps

To a solution of benzamide (1.42 g) in tetrahydrofuran (50 ml) were added sodium hydride (611 mg) and 4-bromobenzenesulfonyl chloride (3.0 g), and the mixture was stirred at room temperature for 3 hours. The mixture was diluted with ethyl acetate and water. The organic layer was separated, washed with brine, dried over magnesium sulfate and evaporated. The residue was purified by column chromatography on silica gel (hexane/ethyl acetate=2/1) to give N-benzoyl-4-bromobenzenesulfonamide (2.1 g) as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037938B2
Source datasetuspto-grants-2006_05
ORD IDord-85d33e726aff4a14a934199ed9221887
Source noteuspto-grants-2006_05