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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444024Generated: October 25, 2026

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

https://huagongshe.com/reaction/444024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-4-(trifluoromethyl)phenolHCID 2736603—
Reactant5-Fluoro-2-nitrobenzamideHCID 18668165—
SolventWaterHCID 962—
Product5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzamideHCID 1533501913.9%

Reaction Steps

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 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04262152
Source datasetuspto-grants-1981_04
ORD IDord-e3d4a52f80c54976b5a67e1a0b5638c5
Source noteuspto-grants-1981_04