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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384460Generated: November 1, 2026

3-Hydroxybenzenethiol → 3-[(tetrahydro-2H-pyran-4-ylmethyl)sulfanyl]phenol

https://huagongshe.com/reaction/384460

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzenethiolHCID 2736613—
Reactant4-(Bromomethyl)oxaneHCID 2773286—
ReactantSodium methanolate methanolHCID 23694274—
SolventMethanolHCID 887—
Product3-[(tetrahydro-2H-pyran-4-ylmethyl)sulfanyl]phenolHCID 5952723759.6%

Reaction Steps

3-Sulfanylphenol (250 mg) was dissolved in methanol (5 mL), and a 28% sodium methoxide-methanol solution (0.5 mL) was added thereto, followed by stirring at room temperature for 10 minutes. 4-(Bromomethyl)tetrahydro-2H-pyrane (410 mg) was added to the reaction mixture, followed by stirring at room temperature for 3 hours. The solvent was evaporated under reduced pressure, and then water was added to the residue, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and dried. The solvent was evaporated under reduced pressure, and the residue was washed with hexane to obtain 3-[(tetrahydro-2H-pyran-4-ylmethyl)sulfanyl]phenol (265 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367702B2
Source datasetuspto-grants-2013_02
ORD IDord-a50ed59e16d641e1a36b653522c88244
Source noteuspto-grants-2013_02