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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128484Generated: October 26, 2026

Potassium Carbonate → Acifluorfen-methyl

https://huagongshe.com/reaction/128484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-4-(trifluoromethyl)phenolHCID 2736603—
Reactant5-Fluoro-2-nitrobenzoic acid methyl esterHCID 5152049—
SolventDimethyl SulfoxideHCID 679—
ProductAcifluorfen-methylHCID 9164284%

Reaction Steps

To a 5-liter, 4-necked flask fitted with a stirrer, thermometer, addition funnel, reflux condenser and drying tube is added dimethyl sulfoxide (200 ml), 2-chloro-4-trifluoromethylphenol) (715 g, 3.64 mole), and anhydrous potassium carbonate (520 g, 3.72 moles). The reaction mixture is stirred at room temperature overnight under a nitrogen atmosphere. Then methyl 5-fluoro-2-nitrobenzoate (724 g, 3.64 moles) is added over a 1 hour period (slight exotherm to 31° C.). After stirring overnight at room temperature, the inorganic solids are removed by filtration and 1700 ml of dimethyl sulfoxide removed under vacuum (1 mm, pot temp. of 85° C., vapor temp. of -40° C.). The residue is diluted with a large volume of carbon tetrachloride and water washed. The organic layer is dried with anhydrous magnesium sulfate and the solvent removed under vacuum to afford 1142 g of methyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate (84% yield). Anal. Calcd. for C15H9ClF3NO5 : C, 47.90; H, 2.42; Cl, 9.45; F, 15.20; N, 3.73. Found: C, 47.83; H, 2.47; Cl, 9.15; L F, 14.84; N, 3.69.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04259510
Source datasetuspto-grants-1981_03
ORD IDord-7d47697a8a054a53b36c6a9edd237aff
Source noteuspto-grants-1981_03