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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288034Generated: October 31, 2026

HCID 23000816, compound → HCID 23000847, compound

https://huagongshe.com/reaction/2288034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23000816HCID 23000816—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 23000847HCID 23000847104.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

In 100 ml of ethanol, 4.68 g (20 mmol) of the resulting 1-benzyl-3-(1-hydroxyethyl)-4-piperidone were dissolved. To the resulting solution, 0.5 g of 5% palladium-carbon were added, followed by stirring at 60° C. for 8 hours under a hydrogen gas atmosphere. After the completion of the reaction, the palladium-carbon was removed by filtration through Celite. The solvent was then distilled off under reduced pressure, whereby 2.98 g of 3-(1-hydroxyethyl)-4-piperidone were obtained as a colorless oil in a quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06087379
Source datasetuspto-grants-2000_07
ORD IDord-e62ac1cbf9f3428a9b2bf063d23c2348
Source noteuspto-grants-2000_07