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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28132Generated: October 30, 2026

Methyl 1-benzyl-4-(phenylamino)piperidine-4-carboxylate → 4-Piperidinecarboxylic acid, 4-(phenylamino)-, methyl ester

https://huagongshe.com/reaction/28132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 1-benzyl-4-(phenylamino)piperidine-4-carboxylateHCID 2724430—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-Piperidinecarboxylic acid, 4-(phenylamino)-, methyl esterHCID 1229817185%

Reaction Steps

A mixture of 32.5 parts of methyl 4-(phenylamino)-1-(phenylmethyl)-4-piperidinecarboxylate and 200 parts of methanol is hydrogenated at normal pressure and at room temperature with 5 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 oily residue solidifies on scratching in 2,2'-oxybispropane. The product is filtered off and dried in vacuo, yielding 20 parts (85%) of methyl 4-(phenylamino)-4-piperidinecarboxylate; mp. 139.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04225606
Source datasetuspto-grants-1980_09
ORD IDord-c6a98fd1a8e24cbcbc0c7a462bfaa154
Source noteuspto-grants-1980_09