Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786713Generated: October 28, 2026

Bromine → Benzenesulfonyl Bromide

https://huagongshe.com/reaction/1786713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantBenzenesulfinic acid, sodium saltHCID 2723840—
ProductBenzenesulfonyl BromideHCID 11138664—

Reaction Steps

Benzenesulfonyl bromide was synthesized with 1316.0 g of the mother liquid containing sodium benzenesulfinate by procedures similar to those of the fourth step and the fifth step of Example 1 except that bromine was used instead of chlorine in the fifth step. Thus, 36.0 g of benzenesulfonyl bromide was yielded. Gas chromatographic analysis revealed that the concentration of benzenesulfonyl bromide in the organic layer was 81.3% (weight; 29.27 g, 0.133 mole), and the yield was 94.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507812B2
Source datasetuspto-grants-2009_03
ORD IDord-18aca290182c4aa0a2257fc9e441bb3d
Source noteuspto-grants-2009_03