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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239824Generated: October 25, 2026

4-Methoxybenzenesulfonyl chloride → N-(2-benzoyl-4-fluoro-phenyl)-4-methoxy-benzenesulfonamide

https://huagongshe.com/reaction/239824

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
Reactant(2-Amino-5-fluorophenyl)(phenyl)methanoneHCID 778082—
ProductN-(2-benzoyl-4-fluoro-phenyl)-4-methoxy-benzenesulfonamideHCID 10430172—

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-fluoro-phenyl)-phenyl-methanone and 101 mg of 4-methoxy-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 3.64 (s, 3H), 6.62 (d, 2H, J=9.2 Hz), 7.02 (m, 1H), 7.25 (m, 1H), 7.31 (m, 2H), 7.37 (m, 2H), 7.48 (m, 2H), 7.56 (m, 1H), 7.79 (q, 1H, J=9.2 Hz, 4.8 Hz), 9.34 (s, 1H). MS: m/z 386.0 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642808B2
Source datasetuspto-grants-2014_02
ORD IDord-8cc914b8e69242a198b6b19426f13095
Source noteuspto-grants-2014_02