Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743852Generated: October 25, 2026

4-Benzyloxy [4-(4-pyridyl)piperazin-2-one-1-yl]benzene → 4-[4-(4-Pyridyl)piperazin-2-one-1-yl]phenol

https://huagongshe.com/reaction/743852

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyloxy [4-(4-pyridyl)piperazin-2-one-1-yl]benzeneHCID 54227295—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product4-[4-(4-Pyridyl)piperazin-2-one-1-yl]phenolHCID 18918415—

Reaction Steps

To a solution of the product of step (i) (1.1 g) in a mixture of methanol (500 ml) and tetrahydrofuran (100 ml) was added 30% palladium-on-charcoal catalyst (300 mg) and the mixture stirred in an atmosphere of hydrogen at ambient temperature and pressure until all the starting material had been consumed. After removal of the catalyst by filtration, the solvent was evaporated in vacuo to give 4-[4-(4-pyridyl)piperazin-2-one-1-yl]phenol as a colourless solid, essentially one spot by tlc, which was used without further purification or characterisation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556977
Source datasetuspto-grants-1996_09
ORD IDord-1e2ddc42f7424b8fbe1cba4ab884d3a6
Source noteuspto-grants-1996_09