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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408132Generated: October 31, 2026

(R)-1-Cbz-3-(Boc(ethyl)amino)piperidine → (R)-3-[Boc(ethyl)amino]piperidine

https://huagongshe.com/reaction/408132

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-1-Cbz-3-(Boc(ethyl)amino)piperidineHCID 86652139—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthanol, mixt. with methanolHCID 18681192—
Product(R)-3-[Boc(ethyl)amino]piperidineHCID 58195511—

Reaction Steps

A solution of (R)-benzyl 3-(tert-butoxycarbonyl(ethyl)amino)piperidine-1-carboxylate (5.00 g, 13.8 mmol) in a mixture of EtOH:MeOH (1:1, 50 mL) was added to a suspension of 10% palladium on activated carbon (1.47 g, 1.38 mmol) in EtOH (20 mL) under N2 atmosphere. The mixture was degassed under N2 (3 cycles) and back filled with H2 (3 cycles) using a H2 balloon. The mixture was then stirred under H2 atmosphere for 4 hours. The reaction mixture was then filtered through a pad of celite washing with 5% MeOH/EtOAc (3×30 mL). The filtrate collected was concentrated in vacuo to provide the crude (R)-tert-butyl ethyl(piperidin-3-yl)carbamate. LCMS (APCI+) m/z 229 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08758830B2
Source datasetuspto-grants-2014_06
ORD IDord-23b4bb9894a143269140182c9a6a5f66
Source noteuspto-grants-2014_06