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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239845Generated: October 25, 2026

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

https://huagongshe.com/reaction/239845

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 numberUS08642808B2
Source datasetuspto-grants-2014_02
ORD IDord-fb94709c1f074dc18b8ad86fd932c0bc
Source noteuspto-grants-2014_02