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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184811Generated: November 1, 2026

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

https://huagongshe.com/reaction/2184811

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(N-Boc-amino)piperidineHCID 4438618—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-(N-Boc-amino)piperidineHCID 723833—

Reaction Steps

6 g of Pd/C (10%) are added to a solution of 0.224 mol of tert-butyl 1-benzyl-4-piperidinylcarbamate in 800 ml of anhydrous ethanol. The reaction mixture is placed under a hydrogen pressure of 4 bars, at 50° C., for 48 hours, and then filtered over Celite and concentrated under reduced pressure, enabling the expected product to be isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399616B1
Source datasetuspto-grants-2002_06
ORD IDord-3932618b9a3347d683f816fe6a35f14e
Source noteuspto-grants-2002_06