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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515415Generated: November 4, 2026

2-Chloro-5-((4-fluoro-phenyl)-hydroxy-methyl)-benzenesulfonamide → 2-Chloro-5-(4-fluoro-benzoyl)-benzenesulfonamide

https://huagongshe.com/reaction/1515415

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-((4-fluoro-phenyl)-hydroxy-methyl)-benzenesulfonamideHCID 58107495—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
Product2-Chloro-5-(4-fluoro-benzoyl)-benzenesulfonamideHCID 5810744374.3%

Reaction Steps

A solution of 65 mg of 2-chloro-5-((4-fluoro-phenyl)-hydroxy-methyl)-benzenesulfonamide in 1 mL of acetone is stirred at room temperature as 0.2 mL of 3 M Jones' reagent is added. The reaction mixture is stirred at room temperature for 30 minutes then diluted with ethyl acetate, filtered through celite, the filtrate is concentrated in vacuo. The crude product is purified by silica gel chromatography to give 48 mg of the title compound as white foam. 1H NMR (CDCl3): 5.15 (br, 2H), 7.12-7.30 (m, 3H), 7.70 (d, J=8 Hz, 1H), 7.80-7.90 (m, 2H), 7.90-8.0 (dd, 1H), 8.5 (d, J=2 Hz, 1H). MS (m/z): 312 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222424B2
Source datasetuspto-grants-2012_07
ORD IDord-a5b2a9e8c9f24f77b750b8d8e12052f6
Source noteuspto-grants-2012_07