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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234364Generated: November 2, 2026

4-(3-Methoxy-4-nitrophenoxy)-1-methylpiperidine → 2-Methoxy-4-((1-methylpiperidin-4-yl)oxy)aniline

https://huagongshe.com/reaction/2234364

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-Methoxy-4-nitrophenoxy)-1-methylpiperidineHCID 57416155—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-Methoxy-4-((1-methylpiperidin-4-yl)oxy)anilineHCID 5523416997.2%

Reaction Steps

To a stirred solution of 4-(3-methoxy-4-nitro-phenoxy)-1-methyl-piperidine (Intermediate 44; 12.86 g, 48.34 mmol) in ethanol (250 mL) under nitrogen was added in one portion the Pd/C catalyst (10%, 1.29 g). The resulting mixture was evacuated and backfilled with nitrogen 4× before hydrogen gas was introduced via a balloon. The reaction mixture was stirred at room temperature for 18 hrs. The catalyst was removed by filtration through celite and the filtrate concentrated under reduced pressure to give a light red oil (11.1 g, 47.0 mmol, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709471B2
Source datasetuspto-grants-2010_05
ORD IDord-66c7bc436e4343aba69fdfd74d1d8d3f
Source noteuspto-grants-2010_05