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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1675163Erstellt: 27. Oktober 2026

1-Benzyloxycarbonyl-4-hydroxy-4-(4-benzyloxyphenyl)piperidine → 4-(4-Hydroxyphenyl)piperidin-4-ol

https://huagongshe.com/reaction/1675163

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Benzyloxycarbonyl-4-hydroxy-4-(4-benzyloxyphenyl)piperidineHCID 21839843—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produkt4-(4-Hydroxyphenyl)piperidin-4-olHCID 1106328166,6%

Reaktionsschritte

10% Palladium on carbon (3.44 g, 3.23 mmol) was added to benzyl 4-[4-(benzyloxy)phenyl]-4-hydroxypiperidine-1-carboxylate (13.49 g, 32.31 mmol) in MeOH (146 mL). The resulting mixture was stirred at room temperature for 20 hours under an atmosphere of hydrogen. The reaction mixture was filtered and evaporated to afford crude product. The crude material was triturated with DCM (100 mL) and MeOH (50 mL) to give a solid which was collected by filtration and dried under vacuum to give 4-(4-hydroxyphenyl)piperidin-4-ol (4.16 g, 66.6%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08003649B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-a2d670071a9a43649afe73022356e1d3
Quellennotizuspto-grants-2011_08