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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128486Generated: October 26, 2026

Water → 5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzamide

https://huagongshe.com/reaction/128486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-4-(trifluoromethyl)phenolHCID 2736603—
ReactantN,N-diethyl-5-fluoro-2-nitrobenzamideHCID 12999068—
SolventDimethyl SulfoxideHCID 679—
SolventBenzene hexaneHCID 110624—
Product5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzamideHCID 1533501981.6%

Reaction Steps

To a 100 ml flask fitted with a magnetic stirrer and drying tube is added dimethyl sulfoxide (30 ml), anhydrous potassium carbonate (7.55 g, 0.054 mole) and 2-chloro-4-trifluoromethylphenol (10.3 g, 0.052 mole). The mixture is stirred at room temperature overnight. A solution of N,N-diethyl-5-fluoro-2-nitrobenzamide (12.5 g, 0.052 mole) in dimethyl sulfoxide (20 ml) is then added rapidly and the reaction mixture is stirred at room temperature for 60 hours. The reaction mixture is poured into water (500 ml) and the product extracted into carbon tetrachloride (4×100 ml), the combined extracts are dried over anhydrous magnesium sulfate and the solvent removed under vacuum to afford 15.3 g of 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzamide (75% yield) Recrystallization from benzene/hexane affords substantially pure product mp. 75°-79° C. Elemental anal, Calcd. for C18H16ClF3N2O4 : C, 51.80; H, 3.88; Cl, 8.55; F, 13.68; N, 6.73. Found: C, 52.03; H, 3.90; Cl, 8.54; F, 13.59; N, 6.83.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04259510
Source datasetuspto-grants-1981_03
ORD IDord-58e228bb23604395be2422d3b310d73b
Source noteuspto-grants-1981_03