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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034628Generated: October 31, 2026

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

https://huagongshe.com/reaction/1034628

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 numberUS08545897B2
Source datasetuspto-grants-2013_10
ORD IDord-40df470a548f45ae99515f1c2cc6df13
Source noteuspto-grants-2013_10