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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237037Generated: October 25, 2026

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

https://huagongshe.com/reaction/2237037

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 numberUS07714013B2
Source datasetuspto-grants-2010_05
ORD IDord-0cb3cf61b9b0441dbeab05830d05a567
Source noteuspto-grants-2010_05