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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283303Generated: October 31, 2026

m-Bromobenzenesulphonyl chloride → HCID 68782055, compound

https://huagongshe.com/reaction/2283303

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Bromobenzenesulphonyl chlorideHCID 17943—
ReactantHCID 68781949HCID 68781949—
SolventPyridineHCID 1049—
ProductHCID 68782055HCID 6878205572.4%

Reaction Steps

To a solution of 2-amino-5-phenoxybenzenesulfonamide (528 mg, 2 mmol) in pyridine (15 mL), 3-bromobenzenesulphonyl chloride (669.3 mg, 2.3 mmol) was added portionwise at 0° C. The reaction was stirred at RT overnight. The pyridine was removed in vacuo and the residue was dissolved in ethyl acetate. The organic phase was washed with aqueous 1N HCl, water and brine, dried over sodium sulfate, and concentrated under reduced pressure. The crude product was purified by flash column chromatography using ethyl acetate/hexane (1:3) as eluent to give the title compound (700 mg, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145380B2
Source datasetuspto-grants-2015_09
ORD IDord-189ef9061ec24529b20271b55cbf7db7
Source noteuspto-grants-2015_09