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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523752Generated: November 1, 2026

Ethanesulfonyl chloride → N-(2-bromophenyl)ethanesulfonamide

https://huagongshe.com/reaction/1523752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanesulfonyl chlorideHCID 11667—
Reactant2-BromoanilineHCID 11992—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductN-(2-bromophenyl)ethanesulfonamideHCID 336298345.4%

Reaction Steps

To a solution of 2-bromoaniline (344 mg, 2.0 mmol) in pyridine (5 mL) was slowly added ethyl-sulfonyl chloride (257 mg, 2.0 mmol) at rt and the mixture was stirred at rt for 16 hours. The pyridine was removed under reduced pressure and resulting residue diluted with water (30 mL) and extracted with DCM (10 mL×2). The combined organic extracts were washed with brine, dried over Na2SO4, filtered and concentrated to dryness. The residue was purified by FCC to give the title compound (240 mg, 45%). MS (ESI): mass calcd. for C8H10BrNO2S 262.96 m/z found 264.1 [M+H]+. 1H NMR (300 MHz, CDCl3) δ 7.71 (dd, J=4.8, 1.5, 1H), 7.59 (dd, J=4.8, 1.5, 1H), 7.32-7.28 (m, 1H), 7.08-7.05 (m, 1H), 6.77 (bs, 1H), 3.14 (q, J=7.2, 2H), 1.41 (t, J=7.5, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079866B2
Source datasetuspto-grants-2015_07
ORD IDord-c2989eec91ee48ef85a4aaf6316e5bb4
Source noteuspto-grants-2015_07