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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575816Generated: October 30, 2026

Hydrochloric Acid → N-(3-bromo-5-phenylmethoxyphenyl)ethanesulfonamide

https://huagongshe.com/reaction/575816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantEthanesulfonyl chlorideHCID 11667—
Reactant3-(Benzyloxy)-5-bromoanilineHCID 57813626—
SolventDichloromethaneHCID 6344—
ProductN-(3-bromo-5-phenylmethoxyphenyl)ethanesulfonamideHCID 11802238394%

Reaction Steps

Ethylsulfonyl chloride (113 uL, 1.2 mmol) was added dropwise to a stirred solution of 3-bromo-5-phenylmethoxyaniline (284 mg, 1.0 mmol) and pyridine (247 uL, 3.1 mmol) in DCM (5 mL) at 0° C. under nitrogen. After the mixture was allowed to warm to rt and stir for 14 h, it was treated with 1N HCl (1 mL) and extracted with DCM (3×5 mL); the combined organic extracts were washed with saturated bicarbonate solution (aq), dried over sodium sulfate, filtered and concentrated in vacuo. The crude solid was purified by silica gel column chromatography using a gradient of EtOAc (5 to 95%) in hexanes to afford the title compound (345 mg, 94%) as an amber oil that solidified upon standing. LCMS (M+H)+=371.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034900B2
Source datasetuspto-grants-2015_05
ORD IDord-5acedd5464de4e048495234164d5054b
Source noteuspto-grants-2015_05