Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 129872Erstellt: 24. Oktober 2026

3,4-Dichlorophenol → 2-(2-Nitro-4-trifluoromethylphenoxy)-4,5-dichlorobenzene

https://huagongshe.com/de/reaction/129872

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,4-DichlorophenolHCID 7258—
Edukt4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotolueneHCID 8462—
EduktPotassium CarbonateHCID 11430—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(2-Nitro-4-trifluoromethylphenoxy)-4,5-dichlorobenzeneHCID 1343009—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A mixture of 3,4-dichlorophenol (25 gram (hereinafter g), 0.153 mol), 4-chloro-3-nitrobenzo-trifluoride (52 g, 0.23 mol) and potassium carbonate (63 g, 0.459 mol) in dimethylformamide (450 mL)was stirred under argon at 120° C. for 24 h. The reaction mixture was filtered and the filtrate evaporated. The residue was dissolved in ethyl acetate, washed with water, brine, dried over anhydrous magnesium sulfate, filtered and evaporated. The residue was flash chromatographed (silica gel, methylene chloride/hexane), to give the title compound as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05470882
Quelldatensatzuspto-grants-1995_11
ORD IDord-2c6a3196267a4fda9525cf2daac82a75
Quellennotizuspto-grants-1995_11