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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18870Generated: October 25, 2026

4-Fluorobenzenesulfonyl chloride → N-(2-benzoyl-4-chlorophenyl)-4-fluorobenzenesulfonamide

https://huagongshe.com/reaction/18870

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
Reactant2-Amino-5-chlorobenzophenoneHCID 12870—
ProductN-(2-benzoyl-4-chlorophenyl)-4-fluorobenzenesulfonamideHCID 5210101—

Reaction Steps

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using 115 mg of (2-amino-5-chloro-phenyl)-phenyl-methanone and 87 mg of 4-fluoro-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 6.90 (t, 1H, J=8.8 Hz, 4.4 Hz), 7.17 (t, 1H, J=7.6 Hz), 7.38-7.46 (m, 5H), 7.52 (d, 2H, J=8 Hz), 7.60 (t, 1H, J=7.2 Hz), 7.70 (d, 1H, J=8.8 Hz), 7.83 (td, 1H, J=8.4, 1.8 Hz), 10.09 (s, 1H). MS: m/z 390.9 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741519B2
Source datasetuspto-grants-2010_06
ORD IDord-8574377c39c14f9fa6336e7f075f38ee
Source noteuspto-grants-2010_06