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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869246Generated: October 30, 2026

Ethanol → Tert-butyl 4-(4-amino-2-methoxyphenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/869246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactanttert-butyl 4-(2-methoxy-4-nitrophenyl)-3,6-dihydropyridine-1(2H)-carboxylateHCID 66642865—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(4-amino-2-methoxyphenyl)piperidine-1-carboxylateHCID 6664290097.3%

Reaction Steps

To a mixture of tert-butyl 4-(2-methoxy-4-nitrophenyl)-3,6-dihydropyridine-1(2H)-carboxylate (Preparation Example 412) (2.21 g), ethanol (40 mL) and THF (20 mL), 10% palladium on carbon (1.0 g) was added and stirred at room temperature for 3 hours under a hydrogen atmosphere at normal pressure. After filtration through celite, the filtrate was distilled off under reduced pressure to give tert-butyl 4-(4-amino-2-methoxy-phenyl)piperidine-1-carboxylate (1.97 g) as a gray solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969336B2
Source datasetuspto-grants-2015_03
ORD IDord-7f75a7bde410467082d2d2ffb377a0bf
Source noteuspto-grants-2015_03