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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837766Generated: October 26, 2026

1-[(2-Methoxy-3-pyridinyl)methyl]-4-[(E)-2-(2-methylphenyl)-1-ethenyl]piperidine → 1-[(2-Methoxy-3-pyridinyl)methyl]-4-[2-(2-methylphenyl)ethyl]piperidine

https://huagongshe.com/reaction/1837766

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[(2-Methoxy-3-pyridinyl)methyl]-4-[(E)-2-(2-methylphenyl)-1-ethenyl]piperidineHCID 22678406—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product1-[(2-Methoxy-3-pyridinyl)methyl]-4-[2-(2-methylphenyl)ethyl]piperidineHCID 2267848397.7%

Reaction Steps

In ethanol (10 ml) was dissolved 473 mg of 1-[(2-methoxy-3-pyridinyl)methyl]-4-[(E)-2-(2-methylphenyl)-1-ethenyl]piperidine. To the mixture was added 100 mg of 10% palladium-carbon powder (water-containing product) was added thereto, followed by stirring at room temperature under normal pressure overnight in a hydrogen atmosphere for 1.5 hours. The reaction solution was filtered, and then the filtrate was evaporated, to give 465 mg of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784192B2
Source datasetuspto-grants-2004_08
ORD IDord-76dd045ba00b4a7e8ea083a1405ac174
Source noteuspto-grants-2004_08