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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177875Generated: November 1, 2026

1-(3-Phenyl-propionyl)-piperidine-4-carboxylic acid benzyl ester → 1-(3-Phenylpropanoyl)piperidine-4-carboxylic acid

https://huagongshe.com/reaction/1177875

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Phenyl-propionyl)-piperidine-4-carboxylic acid benzyl esterHCID 59559625—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product1-(3-Phenylpropanoyl)piperidine-4-carboxylic acidHCID 281319359.7%

Reaction Steps

Pd/c (528 mg) was added to a stirred solution of 1-(3-phenyl-propionyl)-piperidine-4-carboxylic acid benzyl ester (2.64 gm, 7.5 mmol) in MeOH (52.8 mL) and continued the stirring under hydrogen atmosphere for 3 hrs. The mixture was filtered over a bed of celite. The celite was washed with MeOH and the filtrate was concentrated under reduced pressure to afford 1.17 g (59.6% yield) of 1-(3-phenyl-propionyl)-piperidine-4-carboxylic acid. LCMS Purity: 93.56%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-3ff8eea3439b4e4fae466334a638a7c3
Source noteuspto-grants-2010_11