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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203699Generated: October 31, 2026

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

https://huagongshe.com/reaction/2203699

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 numberUS09365568B2
Source datasetuspto-grants-2016_06
ORD IDord-b0009ea7fa9940dcbdcf72f7254393ca
Source noteuspto-grants-2016_06