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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238586Generated: October 30, 2026

4-Fluorobenzenesulfonyl chloride → 4-fluoro-N,N-dimethylbenzenesulfonamide

https://huagongshe.com/reaction/238586

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
ReactantDimethylamine, hydrochlorideHCID 10473—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
Product4-fluoro-N,N-dimethylbenzenesulfonamideHCID 79930150.2%

Reaction Steps

A solution of 4-fluorobenzenesulfonyl chloride (1.95 g, 10 mmol) and dimethylamine hydrochloric acid salt (978 mg, 12 mmol) in tetrahydrofuran (10 mL) was added to a solution of 4-dimethylaminopyridine (3.05 g, 25 mmol) in tetrahydrofuran (10 mL) dropwise at room temperature. The resulting mixture was stirred at room temperature overnight and concentrated in vacuo. The residue was purified by flash column (elution with 20% ethyl acetate in petroleum ether) to afford 4-fluoro-N,N-dimethyl-benzenesulfonamide (1.02 g, 50%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642629B2
Source datasetuspto-grants-2014_02
ORD IDord-c34f281a33e1453d9f9dfb56f45d63b8
Source noteuspto-grants-2014_02