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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448302Generated: November 1, 2026

HCID 12298154, compound → 4-Piperidinecarboxylic acid, 4-[(3-methoxyphenyl)amino]-, methyl ester

https://huagongshe.com/reaction/1448302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12298154HCID 12298154—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-Piperidinecarboxylic acid, 4-[(3-methoxyphenyl)amino]-, methyl esterHCID 12298173—

Reaction Steps

A mixture of 60 parts of methyl 4-[N-(3-methoxyphenyl)amino]-1-(phenylmethyl)-4-piperidinecarboxylate and 400 parts of ethanol is hydrogenated at normal pressure and at room temperature with 10 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen is taken up, the catalyst is filtered off and the filtrate is evaporated. The residue is purified by column-chromatography over silicagel using a mixture of trichloromethane and 10% of methanol, previously saturated with gaseous ammonia, as eluent. The pure fractions are collected and the eluent is evaporated, yielding methyl 4-[N-(3-methoxyphenyl)amino]-4-piperidinecarboxylate as an oily residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179569
Source datasetuspto-grants-1979_12
ORD IDord-a1c59ff51c544c4aa0a979a2bd67c2d7
Source noteuspto-grants-1979_12