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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056292Generated: October 26, 2026

4-t-Butylbenzenesulfonyl chloride → N-(2-benzoyl-4-chloro-3-methoxy-phenyl)-4-tert-butyl-benzenesulfonamide

https://huagongshe.com/reaction/2056292

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-t-Butylbenzenesulfonyl chlorideHCID 139882—
Reactant(6-Amino-3-chloro-2-methoxy-phenyl)-phenyl-methanoneHCID 21107378—
ProductN-(2-benzoyl-4-chloro-3-methoxy-phenyl)-4-tert-butyl-benzenesulfonamideHCID 11385576—

Reaction Steps

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using 131 mg of ((6-Amino-3-chloro-2-methoxy-phenyl)-phenyl-methanone and 116 mg of 4-tert-butyl-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 1.23 (s, 9H), 3.74 (s, 3H), 6.73 (d, 1H, J=2.8 Hz), 7.16 (dd, 1H, J=9.2 Hz, 3.2 Hz), 7.33 (d, 2H, J=8.4 Hz), 7.50 (d, 2H, J=6.0 Hz), 7.56 (d, 2H, J=8.8 Hz), 7.68 (d, 1H, J=9.2 Hz), 8.82 (d, 2H, J=6.4 Hz), 9.38 (s, 1H). MS: m/z 458.1 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335653B2
Source datasetuspto-grants-2008_02
ORD IDord-9c1d0a9ce23d4091a3aaa176c1f6b818
Source noteuspto-grants-2008_02