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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964003Generated: October 30, 2026

HCID 10659313, compound → HCID 10489880, compound

https://huagongshe.com/reaction/964003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10659313HCID 10659313—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 10489880HCID 1048988051.4%

Reaction Steps

A suspension of 4-carbamoyl-1-(4-methoxyphenyl)-pyridinium chloride (22.0 g) in methanol (250 ml) was hydrogenated at ambient temperature and pressure in the presence of 10% palladium-on-carbon catalyst (1.0 g) for 2 days. Further catalyst (0.75 g) was added, and when no more hydrogen was taken up, the catalyst was removed by filtration. The filtrate was basified by the addition of an excess of triethylamine and the solvent removed in vacua. The residue was partitioned between water and a 19:1 mixture of chloroform and methanol. The solvent was removed in vacuo from the organic layer and the residue dried in vacuo over phosphorus pentoxide to give 1-(4-methoxyphenyl)piperidine-4-carboxamide as a white solid (10 g), m.p. 178°-181° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05767116
Source datasetuspto-grants-1998_06
ORD IDord-4cecf59262bd46c7809b99836814d8bd
Source noteuspto-grants-1998_06