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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675163Generated: October 26, 2026

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

https://huagongshe.com/reaction/1675163

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyloxycarbonyl-4-hydroxy-4-(4-benzyloxyphenyl)piperidineHCID 21839843—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-(4-Hydroxyphenyl)piperidin-4-olHCID 1106328166.6%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003649B2
Source datasetuspto-grants-2011_08
ORD IDord-a2d670071a9a43649afe73022356e1d3
Source noteuspto-grants-2011_08