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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064360Generated: October 26, 2026

Tetrahydrofuran → tert-Butyl 4-(3-aminophenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1064360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTert-butyl 4-(3-nitrophenyl)-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 15751429—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventHCID 178418361HCID 178418361—
Producttert-Butyl 4-(3-aminophenyl)piperidine-1-carboxylateHCID 2204926899.7%

Reaction Steps

To a solution of 2.54 g of tert-butyl 1,2,3,6-tetrahydro-4-(3-nitrophenyl)pyridine-1-carboxylate (which was prepared by the method as described in Synthesis, 1991, 993-995) in 20 ml of methanol, 250 mg of 10% palladium-on-carbon catalyst was added, and stirred for an hour in hydrogen atmosphere at ambient temperature and pressure. After addition of 20 ml of tetrahydrofuran to the reaction liquid, the liquid was filtered with Celite. Distilling the solvent off under reduced pressure, 2.30 g of the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969712B2
Source datasetuspto-grants-2005_11
ORD IDord-7da3d97eb32140399b67bb85cf6efebc
Source noteuspto-grants-2005_11