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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15032Generated: October 25, 2026

Tetrahydrofuran → 4-benzyloxy-1-(4-hydroxyphenyl)-1H-pyridin-2-one

https://huagongshe.com/reaction/15032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant4-benzyloxy-1-{4-[tert-butyl(dimethyl)silyloxy]phenyl}-1H-pyridin-2-oneHCID 68430301—
SolventEthyl AcetateHCID 8857—
Product4-benzyloxy-1-(4-hydroxyphenyl)-1H-pyridin-2-oneHCID 6843128399%

Reaction Steps

A THF solution (0.7 mL) of 1N tetrabutylammonium fluoride was added to a THF solution (2 mL) of 4-benzyloxy-1-{4-[tert-butyl(dimethyl)silyloxy]phenyl}-1H-pyridin-2-one (234 mg, 0.573 mmol) and stirred for 30 minutes at room temperature. Ethyl acetate was added to the reaction liquid, the organic layer was washed with water and saturated brine and dried over anhydrous magnesium sulfate. Concentrating the solvent under reduced pressure, the title compound (166 mg, 99%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732456B2
Source datasetuspto-grants-2010_06
ORD IDord-c589eb62117e423e81d087932949699e
Source noteuspto-grants-2010_06