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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17716Generated: October 25, 2026

4-(4-Methoxynaphthalen-1-yloxy)-1-nitrobenzene → 4-(4-Methoxy-naphthalen-1-yloxy)aniline

https://huagongshe.com/reaction/17716

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Methoxynaphthalen-1-yloxy)-1-nitrobenzeneHCID 66977374—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product4-(4-Methoxy-naphthalen-1-yloxy)anilineHCID 66977450—

Reaction Steps

The nitro intermediate (10 mmol) obtained above was dissolved in EtOAc (50 mL) and hydrogenated in the presence of 10% Pd/C (360 mg) until completion according to General Procedure H, as indicated by TLC or HPLC. The reaction mixture was then filtered to remove the catalyst. The solvent was removed in vacuuo to afford the desired 4-(4-methoxy-naphthalen-1-yloxy)aniline, which was used directly for further transformation without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737285B2
Source datasetuspto-grants-2010_06
ORD IDord-8fe4de66f704498f9920a77fee9b4f5c
Source noteuspto-grants-2010_06