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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875618Generated: October 29, 2026

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

https://huagongshe.com/reaction/875618

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 numberUS08981085B2
Source datasetuspto-grants-2015_03
ORD IDord-d45323a972374e359a61c740792a855a
Source noteuspto-grants-2015_03