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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18898Generated: October 25, 2026

Hydrochloric Acid → N-(2-benzoyl-4-chloro-phenyl)-4-iodo-benzenesulfonamide

https://huagongshe.com/reaction/18898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Iodobenzenesulfonyl chlorideHCID 7399—
Reactant2-Amino-5-chlorobenzophenoneHCID 12870—
SolventPyridineHCID 1049—
SolventTolueneHCID 1140—
ProductN-(2-benzoyl-4-chloro-phenyl)-4-iodo-benzenesulfonamideHCID 10028837—

Reaction Steps

To a magnetically stirred solution of 2-amino-5-chlorobenzophenone (1.62 g, 7.0 mmol) in dry pyridine (30 mL) was added dropwise a solution of pipsyl chloride in toluene (12 mL) and the reaction was stirred at ambient temperature. The reaction was added to cold (ice bath) 6M hydrochloric acid with stirring and the mixture was extracted with ethyl acetate (3×50 mL). The extracts were washed with water and with saturated aqueous NaCl. The organic layer was dried (MgSO4), filtered and concentrated to give a crystalline solid. The product was filtered, washed with hexane and dried (vacuum) to get white crystalline solid. 1H NMR (CDCl3) δ 9.63 (br s, 1H, NH), 7,75 (dm, 1H, J=8.8 Hz), 7.62 (tm, 1H, J=7.6 Hz), 7.56 (dm, 1H, J=7.6 Hz), 7.48 (m, 3H), 7.32 (m, 5H). MS: m/z 498.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741519B2
Source datasetuspto-grants-2010_06
ORD IDord-b0a0b1bcdaaa45ae94632dc13858f9ea
Source noteuspto-grants-2010_06