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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397738Generated: October 29, 2026

N-Ethyl-1,2,3,6-tetrahydro-4-(3-(1-methylethoxy)phenyl)pyridine → N-Ethyl-4-(3-(1-methylethoxy)phenyl)piperidine

https://huagongshe.com/reaction/397738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Ethyl-1,2,3,6-tetrahydro-4-(3-(1-methylethoxy)phenyl)pyridineHCID 22707935—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-Ethyl-4-(3-(1-methylethoxy)phenyl)piperidineHCID 2300105799.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

N-Ethyl-1,2,3,6-tetrahydro-4-(3-(1-methylethoxy)phenyl)pyridine (Preparation 44, 2.0 g, 8.16 mmol) was dissolved in ethanol (20 ml) and 5% palladium on carbon (0.2 g) was added. The suspension was heated at 60° C. under hydrogen (20 psi) for 5 h. The mixture was cooled and the solid was removed by filtration through Arbocel™, washing the resultant cake with ethyl acetate. The filtrate was concentrated in vacuo to give the title compound as an oil (2.0 g, 99%) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610711B2
Source datasetuspto-grants-2003_08
ORD IDord-a7bd88c9793b452192f3e6a0804da337
Source noteuspto-grants-2003_08