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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239815Generated: October 26, 2026

2-Amino-5-chlorobenzophenone → N-(2-benzoyl-4-chlorophenyl)-4-tert-butylbenzenesulfonamide

https://huagongshe.com/reaction/239815

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-chlorobenzophenoneHCID 12870—
Reactant4-t-Butylbenzenesulfonyl chlorideHCID 139882—
ProductN-(2-benzoyl-4-chlorophenyl)-4-tert-butylbenzenesulfonamideHCID 1732024—

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 116 mg of 4-tert-Butyl-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 1.21 (s, 9H), 7.28-7.34 (m, 3H), 7.37-7.44 (m, 4H), 7.48 (dd, 1H, J=8.8, 2.4 Hz), 7.54-7.62 (m, 3H), 7.78 (d, 1H, J=8.8 Hz), 9.89 (s, 1H). MS: m/z 428.9 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642808B2
Source datasetuspto-grants-2014_02
ORD IDord-424caa4f860d433c90d8093a1b64ae42
Source noteuspto-grants-2014_02