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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174690Generated: October 29, 2026

1-(4-Nitrophenyl)-4-piperidinol → 1-(4-Aminophenyl)piperidin-4-ol

https://huagongshe.com/reaction/2174690

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Nitrophenyl)-4-piperidinolHCID 613768—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Aminophenyl)piperidin-4-olHCID 16792107—

Reaction Steps

The 4-hydroxy-N-(4-nitrophenyl)piperidine (11.1 g, 50 mmol) obtained in Example 1(1) was dissolved in methanol (100 ml) and tetrahydrofuran (50 ml), and 10% palladium-carbon (8.0 g) was added thereto, followed by stirring at room temperature in an atmosphere of hydrogen gas for 7 hours. After the insoluble material was filtered with Celite, the filtrate was concentrated under reduced pressure, diethyl ether was added to the obtained residue, and the precipitate was collected by filtration, thereby obtaining 4-hydroxy-N-(4-aminophenyl)piperidine (9.25 g, 94%) as a reddish-purple solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062035B2
Source datasetuspto-grants-2015_06
ORD IDord-731e86c56005461fa1580c79a81e2c8e
Source noteuspto-grants-2015_06