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HRID 1940719作成日:2026年10月25日

Dimethylformamide → 3-(2-chloro-6-fluorophenyl)-5-[3-chloro-4-(4-trifluoromethylphenoxymethyl)phenyl]-1-methyl-1H-1,2,4-triazole

https://huagongshe.com/reaction/1940719

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物4-(Trifluoromethyl)phenolHCID 67874—
反応物5-(4-bromomethyl-3-chlorophenyl) 3-(2-chloro-6-fluorophenyl)-1-methyl-1H-1,2,4-triazoleHCID 21463648—
溶媒WaterHCID 962—
生成物3-(2-chloro-6-fluorophenyl)-5-[3-chloro-4-(4-trifluoromethylphenoxymethyl)phenyl]-1-methyl-1H-1,2,4-triazoleHCID 2146358878.4%

反応手順

To 30 ml of N,N-dimethylformamide are added 4-trifluoromethyl phenol (0.77 g) and potassium carbonate (0.72 g) and 5-(4-bromomethyl-3-chlorophenyl)-3-(2-chloro-6-fluorophenyl)-1-methyl-1H-1,2,4-triazole (1.60 g) is added thereto at room temperature with stirring, which is stirred at 120° C. for 1 hour. On completion of the reaction, the reaction solution is cooled to room temperature, poured into water and extracted with toluene. The organic layer is washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The concentrate is purified by silica gel column chromatography to give 1.50 g of desired compound (refractive index: 1.5961).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05700824
出典データセットuspto-grants-1997_12
ORD IDord-5fe1170c6854469984f2226910a6de34
出典メモuspto-grants-1997_12