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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 743852Erstellt: 23. Oktober 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/de/reaction/743852

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Benzyloxy [4-(4-pyridyl)piperazin-2-one-1-yl]benzeneHCID 54227295—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-[4-(4-Pyridyl)piperazin-2-one-1-yl]phenolHCID 18918415—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05556977
Quelldatensatzuspto-grants-1996_09
ORD IDord-1e2ddc42f7424b8fbe1cba4ab884d3a6
Quellennotizuspto-grants-1996_09