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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237033Generated: October 30, 2026

2-(4-Nitrophenoxy)naphthalene → 2-(4-Aminophenoxy)naphthalene

https://huagongshe.com/reaction/2237033

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Nitrophenoxy)naphthaleneHCID 762478—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-(4-Aminophenoxy)naphthaleneHCID 3580829—

Reaction Steps

The nitro intermediate (10 mmol) obtained above was dissolved in EtOH (50 mL) and hydrogenated in the presence of 10% Pd/C (300 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-(naphthalen-2-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-0f6bda796f7948ffa4f1914388480419
Source noteuspto-grants-2010_05