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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248796Generated: October 27, 2026

Methyl 3-methyl-4-[(phenylmethyl)amino]-1-piperidinecarboxylate → Methyl 4-amino-3-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/2248796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-methyl-4-[(phenylmethyl)amino]-1-piperidinecarboxylateHCID 19785254—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 4-amino-3-methylpiperidine-1-carboxylateHCID 19785295—

Reaction Steps

A mixture of 40 parts of methyl 3-methyl-4-[(phenylmethyl)amino]-1-piperidinecarboxylate and 160 parts of methanol was hydrogenated at normal pressure and at room temperature with 2 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated to dry. The residue was distilled (bp. 80° C. at 0.1 mm. pressure). The distillate was further purified by gas-chromatography (at 215° C. and at 10 lbs/sq. inch), yielding 8.6 parts of methyl 4-amino-3-methyl-1-piperidinecarboxylate (interm. 27)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041448
Source datasetuspto-grants-1991_08
ORD IDord-b634badc0828420e89e1f1d436b841b9
Source noteuspto-grants-1991_08