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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409734Generated: October 26, 2026

4-(4-Ethoxyphenyl)pyridine → 4-(4-Ethoxyphenyl)piperidine

https://huagongshe.com/reaction/409734

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Ethoxyphenyl)pyridineHCID 70700933—
CatalystAdams' catalystHCID 345198—
SolventAcetic AcidHCID 176—
Product4-(4-Ethoxyphenyl)piperidineHCID 21495191—
ProductTHF MeOH NH4OHHCID 86686122—

Reaction Steps

410 mg (2.06 mmol) 4-(4-Ethoxy-phenyl)-pyridine in 10 mL acetic acid are hydrogenated (3 bar) for 9 h at rt using 50 mg platinum(IV) oxide. After that time, the catalyst is filtered off and the solvent is evaporated. The residue is taken up in 1N NaOH and extracted with EtOAc. The organic layer is dried over sodium sulphate and the solvent is evaporated. The residue is purified by column chromatography (silica gel; DCM:MeOH 9:1, then THF:MeOH:NH4OH 1:1:0.1) to yield the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759528B2
Source datasetuspto-grants-2014_06
ORD IDord-db7752a720184053b3748059490b60bf
Source noteuspto-grants-2014_06