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HRID 128486作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/128486

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物2-Chloro-4-(trifluoromethyl)phenolHCID 2736603—
反応物N,N-diethyl-5-fluoro-2-nitrobenzamideHCID 12999068—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Benzene hexaneHCID 110624—
生成物5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzamideHCID 1533501981.6%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04259510
出典データセットuspto-grants-1981_03
ORD IDord-58e228bb23604395be2422d3b310d73b
出典メモuspto-grants-1981_03