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HRID 444026作成日:2026年10月26日

Potassium Carbonate → Acifluorfen-methyl

https://huagongshe.com/reaction/444026

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Methyl 5-chloro-2-nitrobenzoateHCID 171018—
反応物2-Chloro-4-(trifluoromethyl)phenolHCID 2736603—
溶媒Dimethyl SulfoxideHCID 679—
生成物Acifluorfen-methylHCID 91642—

反応条件

温度50 °C

反応手順

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-4trifluoromethylphenoxy)-2-nitrobenzoate which is determined by spectral data to be identical with the product of Example 1B.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04262152
出典データセットuspto-grants-1981_04
ORD IDord-5e29b6c33ba1463499fc2939fde75b05
出典メモuspto-grants-1981_04