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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354033Generated: October 30, 2026

Piperidine → 4-(Piperidin-1-yl)phenol

https://huagongshe.com/reaction/2354033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant1,4-CyclohexanedioneHCID 12511—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product4-(Piperidin-1-yl)phenolHCID 9045243.4%

Reaction Steps

0.85 g of piperidine, 1.68 g of 1,4-cyclohexanedione and 40 mg of 10% palladium-carbon were heated with stirring in 40 ml of ethanol at 50° C. to 60° C. and reacted for 8 hours under air bubbling. During the reaction, ethanol was added as needed. After the completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated under reduced pressure. The resultant was purified by silica gel column chromatography (n-hexane:ethyl acetate=4:1) and purified by silica gel column chromatography again, and 0.668 g of 1-(4-hydroxyphenyl)piperidine was obtained (yield 43.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750156B2
Source datasetuspto-grants-2010_07
ORD IDord-4d0f3a4a48f44ec1ad5e42423237ca77
Source noteuspto-grants-2010_07