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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17712Generated: October 25, 2026

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

https://huagongshe.com/reaction/17712

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 numberUS07737285B2
Source datasetuspto-grants-2010_06
ORD IDord-3a02678eca04486f9c195a6aa83690bd
Source noteuspto-grants-2010_06