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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116468Generated: October 31, 2026

m-Bromobenzenesulphonyl chloride → 3-Bromobenzene-1-sulfonyl fluoride

https://huagongshe.com/reaction/2116468

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Bromobenzenesulphonyl chlorideHCID 17943—
ReactantPotassium FluorideHCID 522689—
Catalyst18-Crown-6HCID 28557—
SolventAcetonitrileHCID 6342—
Product3-Bromobenzene-1-sulfonyl fluorideHCID 7070003981%

Reaction Steps

To a stirred solution of 3-bromophenylsulfonyl chloride (5 g, 0.0196 mol) in acetonitrile (20 ml) was added potassium fluoride (2.27 g, 0.0391 mol) followed by 18-crown-6 ether (0.08 g) and the reaction stirred at room temperature for 18 h. The reaction mixture was then washed with water (60 ml), extracted with ethyl acetate (3×80 ml) and the combined organic extracts dried (Na2SO4). Solvents were evaporated in vacuo to give a yellow oil (3.79 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439245B2
Source datasetuspto-grants-2008_10
ORD IDord-9e3770c8371746d9a4487f5b74a4a18e
Source noteuspto-grants-2008_10