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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1950749Generated: October 25, 2026

1-Cyclopropyl-4-(4-nitrophenyl)piperidine → 4-(1-Cyclopropylpiperidin-4-yl)aniline

https://huagongshe.com/reaction/1950749

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Cyclopropyl-4-(4-nitrophenyl)piperidineHCID 68672156—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product4-(1-Cyclopropylpiperidin-4-yl)anilineHCID 68672941—

Reaction Steps

0.57 g 1-cyclopropyl-4-(4-nitro-phenyl)-piperidine are dissolved in 30 mL tetrahydrofuran and combined with Pd/C. The mixture is hydrogenated for 72 h at 7 bar hydrogen pressure. Then the catalyst is filtered off and the solvent is eliminated in vacuo. The residue is used in the next stage of the synthesis without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404674B2
Source datasetuspto-grants-2013_03
ORD IDord-f55b8c37592e45d989c6a93a135b05a9
Source noteuspto-grants-2013_03