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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480201Generated: October 29, 2026

Thiophenol → 5-Chloro-2-hydroxy-N-methyl-benzenesulfonamide

https://huagongshe.com/reaction/480201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantSodium hydrideHCID 24758—
Reactant5-chloro-2-methoxy-N-methylbenzenesulfonamideHCID 2987885—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-Chloro-2-hydroxy-N-methyl-benzenesulfonamideHCID 1876810264.2%

Reaction Steps

To a solution of sodium hydride (60% in mineral oil, 90.24 mg, 2.25 mmol) in dry dimethyl formamide was added thiophenol (0.225 ml, 2.25 mmol) dropwise. To this was then added 5-Chloro-2-methoxy-N-methyl-benzenesulfonamide (531 mg, 2.25 mmol) followed by refluxing for 4 hours. The reaction mixture was cooled, diluted with ethyl acetate and washed with a 1N sulfuric acid solution. The organic layer was separated, dried over magnesium sulfate, filtered and concentrated in vacuo. Chromatography on silica gel yielded the above titled compound (320 mg, 53% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06649611B2
Source datasetuspto-grants-2003_11
ORD IDord-8d3749d4f25943e7b04a0ddc71f49585
Source noteuspto-grants-2003_11