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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283324Generated: November 1, 2026

m-Bromobenzenesulphonyl chloride → HCID 57751032, compound

https://huagongshe.com/reaction/2283324

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Bromobenzenesulphonyl chlorideHCID 17943—
Reactant2-AminobenzenesulfonamideHCID 72894—
SolventDiethyl EtherHCID 3283—
ProductHCID 57751032HCID 5775103248%

Reaction Steps

The title compound was synthesized as described for Example 178 in 48% yield, starting from 2-aminobenzenesulfonamide and 3-bromobenzenesulfonyl chloride. The product solidified after the extractive work up. Diethyl ether (25 mL) was added and the crystals were crushed with a glass stick. The mixture was filtered and the solid was rinsed with diethyl ether and dried in vacuo at ambient temperature.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145380B2
Source datasetuspto-grants-2015_09
ORD IDord-530f2fd906f049bd85bcd615e7dd4551
Source noteuspto-grants-2015_09