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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872882Generated: November 1, 2026

4-(4-Fluorophenoxy)benzenesulphonyl chloride → 4-(4-Fluorophenoxy)benzene-1-thiol

https://huagongshe.com/reaction/1872882

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Fluorophenoxy)benzenesulphonyl chlorideHCID 2782757—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Fluorophenoxy)benzene-1-thiolHCID 21705585100%

Reaction Steps

Lithium aluminum hydride (9.95 grams, 0.26 mole) was added in portions to a stirred solution of 4-(4-fluorophenoxy)benzenesulfonylchloride (30 grams, 0.105 mole) in tetrahydrofuran (700 mL). The resulting mixture was heated at reflux for 1.5 hours, cooled in an ice bath and quenched by addition of 10% aqueous sulfuric acid solution (100 mL). After stirring for 30 minutes, the mixture was filtered through Celite™ and the tetrahydrofuran was removed under vacuum. The residue was diluted with water and extracted with diethyl ether. The organic layer was washed with water and brine, dried over magnesium sulfate and concentrated under vacuum to provide the title compound as a white solid (23 grams, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06110964
Source datasetuspto-grants-2000_08
ORD IDord-349d59eb47f4417e8157bb11153bff4a
Source noteuspto-grants-2000_08