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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846777Generated: October 25, 2026

1-Phenethylamine → (+)-Ethyl cis-3-methoxy-4-[(1-phenylethyl)amino]-1-piperidinecarboxylate

https://huagongshe.com/reaction/846777

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenethylamineHCID 7408—
ReactantThiopheneHCID 8030—
ReactantEthyl 3-methoxy-4-oxopiperidine-1-carboxylateHCID 2724451—
Reactant1-[4-(chloromethyl)phenyl]-1H-imidazole hydrochlorideHCID 19794662—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
Product(+)-Ethyl cis-3-methoxy-4-[(1-phenylethyl)amino]-1-piperidinecarboxylateHCID 6791457651%

Reaction Steps

A solution of 20 parts of ethyl 3-methoxy-4-oxo-1-piperidinecarboxylate, 12 parts of (-)-α-methylbenzenemethanamine, 2 parts of a solution of thiophene in ethanol 4% and 200 parts of methanol was hydrogenated at normal pressure and at room temperature with 4 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 in vacuo. The residue was purified by HPLC using a mixture of hexane, trichloromethane and methanol (50:49.5:0.5 by volume) as eluent. The pure A-fractions were collected and the eluent was evaporated, yielding 15.62 parts (51%) of (-)-ethyl cis-3-methoxy-4-[(1-phenylethyl)-amino]-1-piperidinecarboxylate as a residue (intermediate 103).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137896
Source datasetuspto-grants-1992_08
ORD IDord-a02a987b80b84a61903307b9f59a9679
Source noteuspto-grants-1992_08