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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814810Generated: November 2, 2026

1-Benzyl-4-(N-Boc-amino)piperidine → 4-(N-Boc-amino)piperidine

https://huagongshe.com/reaction/1814810

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(N-Boc-amino)piperidineHCID 4438618—
SolventEthanolHCID 702—
SolventPalladiumHCID 23938—
Product4-(N-Boc-amino)piperidineHCID 72383395.2%

Reaction Steps

1-Benzyl-4-t-butyloxycarbonylaminopiperidine (Method D, 5.4 g, 18.6 mmol) was dissolved in absolute ethanol (100 ml) and hydrogenated over 10% Pd/C for 24 hours at ambient temperature. The catalyst was removed by filtration and the filtrates evaporated to give the title compound (3.54 g, 17.7 mmol) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878712B1
Source datasetuspto-grants-2005_04
ORD IDord-e4e21712af8b4dd390e165f5b87dea96
Source noteuspto-grants-2005_04