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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17672Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/17672

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzeneHCID 66977640—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produkt4-[4-Fluoro-3-(trifluoromethyl)phenoxy]anilineHCID 6697734495%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737285B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-6c7836f1096640248aaaa4d77fde89eb
Quellennotizuspto-grants-2010_06