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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386767Generated: November 1, 2026

1-(Benzyloxycarbonyl)-4-(3-oxo-3-phenylprop-1-enyl)piperidine → 1-(Benzyloxycarbonyl)-4-(3-oxo-3-phenylpropyl)piperidine

https://huagongshe.com/reaction/1386767

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Benzyloxycarbonyl)-4-(3-oxo-3-phenylprop-1-enyl)piperidineHCID 57074489—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-(Benzyloxycarbonyl)-4-(3-oxo-3-phenylpropyl)piperidineHCID 18187454100.1%

Reaction Steps

1-(Benzyloxycarbonyl)-4-(3-oxo-3-phenylprop-1-enyl)piperidine (0.95 g, 2.7 mmol, from EXAMPLE 154, Step A) was hydrogenated using 5% Pd/C (10 mg) in 95% ethanol (20 mL) at atmospheric pressure. After 3.5 h, the mixture was filtered and the catalyst was washed with 95% ethanol. Evaporation of the filtrate gave 0.95 g of 1-(benzyloxycarbonyl)-4-(3-oxo-3-phenylpropyl)piperidine as a colorless syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265434B1
Source datasetuspto-grants-2001_07
ORD IDord-e18aafbc93e846b4bd1a7bdeb3c36a10
Source noteuspto-grants-2001_07