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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17667Erstellt: 24. Oktober 2026

Water → 1-Fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzene

https://huagongshe.com/de/reaction/17667

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Eduktp-FluoronitrobenzeneHCID 9590—
EduktPotassium CarbonateHCID 11430—
Edukt4-Fluoro-3-(trifluoromethyl)phenolHCID 601854—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzeneHCID 66977640—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a stirred solution of 4-fluoronitrobenzene (20 mmol), 4-fluoro-3-trifluoromethylphenol (22 mmol) in DMF (50 mL) at rt, solid potassium carbonate (60 mmol) was added, and the reaction mixture was heated to 90° C. for 5 h (monitored by TLC), according to General Procedure L1. After cooling to rt, the reaction mixture was poured into cold H2O (60 mL). The resulting mixture was extracted with EtOAc (3×100 mL). The combined EtOAc extracts were washed with H2O (2×40 mL) and brine (50 mL), and dried over anhydrous sodium sulfate. The solvent was removed in vacuuo to afford the desired 1-fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzene. The crude product was used directly for further transformation without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737285B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-1bd30d5ef1eb4a5b8490b5a438d26268
Quellennotizuspto-grants-2010_06