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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 128485Erstellt: 24. Oktober 2026

Dimethyl Sulfoxide → 5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzamide

https://huagongshe.com/de/reaction/128485

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktPotassium CarbonateHCID 11430—
Edukt2-Chloro-4-(trifluoromethyl)phenolHCID 2736603—
Edukt5-Fluoro-2-nitrobenzamideHCID 18668165—
LösungsmittelWaterHCID 962—
Produkt5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzamideHCID 1533501913,9%

Reaktionsschritte

To a 100 ml flask fitted with a magnetic stirrer and drying tube is added dimethyl sulfoxide (50 ml), anhydrous potassium carbonate (3.6 g, 0.026 mole) and 2-chloro-4-trifluoromethylphenol (4.8 L g, 0.024 mole). This mixture is stirred at room temperature overnight. 5-Fluoro-2-nitrobenzamide (4.5 g, 0.024 mole) is added rapidly and the reaction mixture stirred at room temperature for 24 hours. The reaction mixture is poured into water (300 ml) and triturated with carbon tetrachloride (50 ml). The water and carbon tetrachloride insoluble solid is collected by filtration and dried under vacuum to afford 1.2 g of 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzamide, mp 139°-43° C. Anal. Calcd. for C14H8ClF3N2O4 : C, 46.62; H, 2.23; Cl, 9.83; N, 7.76. Found: C, 45.77; H, 2.30; Cl, 10.62; N, 7.91.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04259510
Quelldatensatzuspto-grants-1981_03
ORD IDord-f80b141f54f940a7864c26280652765b
Quellennotizuspto-grants-1981_03