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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773314Generated: November 3, 2026

Ethyl 1-benzyl-4-oxopiperidine-3-carboxylate → 4-Oxo-piperidine-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1773314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-benzyl-4-oxopiperidine-3-carboxylateHCID 102624—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-Oxo-piperidine-3-carboxylic acid ethyl esterHCID 10731688.4%

Reaction Steps

To a solution of ethyl 1-benzyl-4-oxopiperidine-3-carboxylate (360.0 g, 1.21 mol) in EtOH (6.7 L) was added wet Pd/C (55.0 g) under N2 that then was replaced by H2. The reaction mixture was stirred at rt for 4 h, filtered and concentrated to give a crude product. The crude product was slurried with EtOH (200 mL) for 2 h and then filtered. The filtered cake was washed with MTBE and the combined organic phases were concentrated to give the title compound (222.0 g, 1.07 mol, 88.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255096B1
Source datasetuspto-grants-2016_02
ORD IDord-e33d861d862540c89f7e6b56f0a739a1
Source noteuspto-grants-2016_02