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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042699Generated: November 1, 2026

1-[3-(4-Nitrophenoxy)propyl]piperidine → 4-[3-(1-Piperidinyl)propoxy]aniline

https://huagongshe.com/reaction/1042699

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[3-(4-Nitrophenoxy)propyl]piperidineHCID 2057928—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-[3-(1-Piperidinyl)propoxy]anilineHCID 21974932—

Reaction Steps

A mixture of 1-[3-(4-nitrophenoxy)propyl]piperidine (15.5 g, 58.6 mmol) and 10% Pd/C (12.5 g) in 150 mL of EtOH was placed under a balloon of H2. The mixture was stirred for 18 h. The catalyst was removed by suction filtration and the organics concentrated to give the title compound as a yellowish oil. MS (m/z)=235.2 (M+H+); Calc'd for C14H22N2O=234.34.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557996B2
Source datasetuspto-grants-2013_10
ORD IDord-347ff4b37e814d10908bdb0e5b368340
Source noteuspto-grants-2013_10