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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17668Generated: October 26, 2026

1-Fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzene → 4-[4-Fluoro-3-(trifluoromethyl)phenoxy]aniline

https://huagongshe.com/reaction/17668

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzeneHCID 66977640—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-[4-Fluoro-3-(trifluoromethyl)phenoxy]anilineHCID 6697734495%

Reaction Steps

The nitro intermediate (2 mmol) obtained above was dissolved in MeOH (10 mL) and hydrogenated in the presence of 10% Pd/C (50 mg) until completion as indicated by TLC or LC-MS, according to General Procedure H. The reaction mixture was then filtered to remove the catalyst. The solvent was removed in vacuuo to afford 4-(4′-fluoro-3′-trifluoromethyl-phenoxy)aniline, which was used directly for further transformation without purification (overall yield: 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737285B2
Source datasetuspto-grants-2010_06
ORD IDord-d607a5691d4945faa36d1f0ad5c72ab5
Source noteuspto-grants-2010_06