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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448305Generated: November 2, 2026

HCID 12298160, compound → 4-Piperidinecarboxylic acid, 4-[(4-fluorophenyl)amino]-, methyl ester

https://huagongshe.com/reaction/1448305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12298160HCID 12298160—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-Piperidinecarboxylic acid, 4-[(4-fluorophenyl)amino]-, methyl esterHCID 12298178—

Reaction Steps

A mixture of 53 parts of methyl 4-[(4-fluorophenyl)amino]-1-(phenylmethyl)-4-piperidinecarboxylate and 400 parts of methanol 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 silica gel using a mixture of trichloromethane and 15% of methanol, previously saturated with gaseous ammonia, as eluent. The pure fractions are collected and the eluent is evaporated. The oily residue solidifies on scratching in hexane. The product is filtered off and dried, yielding methyl 4-[(4-fluorophenyl)amino]-4-piperidinecarboxylate; mp. 83.7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179569
Source datasetuspto-grants-1979_12
ORD IDord-1d5f2e1fb36145b4afe534a96e1b642c
Source noteuspto-grants-1979_12