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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276887Generated: October 30, 2026

tert-butyl 4-(2-methoxyphenyl)-5,6-dihydropyridine-1(2H)-carboxylate → Tert-butyl 4-(2-methoxyphenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/276887

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-(2-methoxyphenyl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 22629561—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductTert-butyl 4-(2-methoxyphenyl)piperidine-1-carboxylateHCID 2262956779.2%

Reaction Steps

1-t-Butoxycarbonyl-4-(2-methoxyphenyl)-1,2,3,6-tetrahydropyridine (150 mg, 0.52 mmol) and 10% palladium-carbon (30 mg) were stirred in methanol for two nights in an atmosphere of hydrogen. The reaction solution was filtered and the thus obtained residue was thoroughly washed with methanol. Then the filtrate and washed solution were combined and evaporated under a reduced pressure to obtain 120 mg of the aforementioned compound of interest (0.42 mmol, 81% in yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355642B1
Source datasetuspto-grants-2002_03
ORD IDord-1c93181ed6c141e88aedf99d29168dff
Source noteuspto-grants-2002_03