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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371131Generated: November 1, 2026

Benzyl 4-{[(3R)-1-ethylpiperidin-3-yl]methyl}piperazine-1-carboxylate → 1-{[(3R)-1-ethylpiperidin-3-yl]methyl}piperazine

https://huagongshe.com/reaction/2371131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-{[(3R)-1-ethylpiperidin-3-yl]methyl}piperazine-1-carboxylateHCID 57656880—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-{[(3R)-1-ethylpiperidin-3-yl]methyl}piperazineHCID 57656847104.5%

Reaction Steps

Benzyl 4-{[(3R)-1-ethylpiperidin-3-yl]methyl}piperazine-1-carboxylate (352 mg) was dissolved in ethanol (50 ml). 10% Palladium on carbon (35 mg) was added and the mixture stirred for 18 hours at room temperature under an atmosphere of hydrogen. The reaction mixture was filtered through a pad of celite and the filtrate concentrated in vacuo to give the title compound (225 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710224B2
Source datasetuspto-grants-2014_04
ORD IDord-095f7f67f4844c068750d3bffb00e080
Source noteuspto-grants-2014_04