Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901701Generated: October 27, 2026

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

https://huagongshe.com/reaction/901701

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 numberUS07361678B2
Source datasetuspto-grants-2008_04
ORD IDord-4098d2e63ca645a590fc95b97a372b7b
Source noteuspto-grants-2008_04