Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18896Generated: October 25, 2026

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

https://huagongshe.com/reaction/18896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
Reactant2-Amino-5-chlorobenzophenoneHCID 12870—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductN-(2-benzoyl-4-chloro-phenyl)-4-bromo-benzenesulfonamideHCID 333475798.4%

Reaction Steps

2-Amino-5-chlorobenzophenone (5.33 g, 23 mmol) was dissolved in 100 mL pyridine and stirred at room temperature. 4-Bromobenzenesulfonyl chloride (6.17 g, 24.1 mmol) was added and the mixture was stirred overnight. The mixture was poured in a steady stream into 350 mL vigorously stirring chilled 6M HCl which resulted in the precipitation of a reddish oil. The solution was diluted with 100 mL EtOAc and 200 mL H2O, shaken in a separating funnel and the aqueous layer discarded. The organics were dried and reduced in vacuo to yield title compound (10.2 g, 98%). 1H NMR (400 MHz, CDCl3): δ 7.34 (m, 5H), 7.43-7.48 (m, 5H), 7.62 (t, 1H), 7.74 (d, 1H), 9.62 (s, 1H). MS: m/z=449.9 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741519B2
Source datasetuspto-grants-2010_06
ORD IDord-26c50f35ca01425f953f3b1789ffe2e9
Source noteuspto-grants-2010_06