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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981300Generated: October 30, 2026

Thiophene → Ethyl trans-3-hydroxy-4-[methyl(phenylmethyl)amino]-1-piperidinecarboxylate

https://huagongshe.com/reaction/981300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantEthyl trans-3-hydroxy-4-[(phenylmethyl)amino]-1-piperidinecarboxylateHCID 13677850—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178486302HCID 178486302—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductEthyl trans-3-hydroxy-4-[methyl(phenylmethyl)amino]-1-piperidinecarboxylateHCID 6792874579.9%

Reaction Steps

(a-2) A mixture of 40 parts of ethyl trans-3-hydroxy-4-[(phenylmethyl)-amino]-1-piperidinecarboxylate, 15 parts of poly(oxymethylene), 2 parts of a solution of thiophene in methanol and 400 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. The residue was dissolved in trichloromethane. The organic layer was washed successively with a dilute ammonium hydroxide solution and water, dried, filtered and evaporated in vacuo. The residue was crystallized from 80 parts of acetonitrile The product was filtered off and dried, yielding 32.7 parts (79.9%) of ethyl trans-3-hydroxy-4-[methyl(phenylmethyl)amino]-1-piperidinecarboxylate (interm. 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04990521
Source datasetuspto-grants-1991_02
ORD IDord-1c974843383849e2b1c7b21b0f604ab4
Source noteuspto-grants-1991_02