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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128487Generated: October 25, 2026

Potassium Carbonate → Acifluorfen-methyl

https://huagongshe.com/reaction/128487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-chloro-2-nitrobenzoateHCID 171018—
Reactant2-Chloro-4-(trifluoromethyl)phenolHCID 2736603—
SolventDimethyl SulfoxideHCID 679—
ProductAcifluorfen-methylHCID 91642—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a flask fitted with a drying tube is charged DMSO (10 ml), 2-chloro-4-trifluoromethylphenol (3.93 g, 0.02 mole) and anhydrous potassium carbonate (2.76 g, 0.02 mole). Then methyl 5-chloro-2-nitrobenzoate (4.3 g, 0.02 mole) is added and the reaction mixture warmed to 50° C. for 3 hours. (Gas-liquid chromatography analysis suggested a low conversion to desired product.) The temperature is raised to 60° C. for 16 hours and then to 70° C. for 16 hours. Additional potassium carbonate (1.38 g, 0.01 mole) is added and heating at 70° C. is continued for an additional 5 days, the reaction mixture is cooled to room temperature, poured into a benzene/hexane cosolvent and extracted twice with water. The organic layer is dried with anhydrous sodium sulfate, filtered and the solvent removed under vacuum (110° C., 0.1 mm) to afford 2.0 g, (27% yield) of methyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate which is determined by spectral data to be identical with the product of Example 1B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04259510
Source datasetuspto-grants-1981_03
ORD IDord-2388b8ffa0314366993583946d76afeb
Source noteuspto-grants-1981_03