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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810144Generated: November 1, 2026

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

https://huagongshe.com/reaction/1810144

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 numberUS08362063B2
Source datasetuspto-grants-2013_01
ORD IDord-021c5eb3bbb542eaa13848f86e5774e7
Source noteuspto-grants-2013_01