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HRID 129872作成日:2026年10月26日

3,4-Dichlorophenol → 2-(2-Nitro-4-trifluoromethylphenoxy)-4,5-dichlorobenzene

https://huagongshe.com/reaction/129872

反応式

関与物質

役割名称HCID仕込み量
反応物3,4-DichlorophenolHCID 7258—
反応物4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotolueneHCID 8462—
反応物Potassium CarbonateHCID 11430—
溶媒DimethylformamideHCID 6228—
生成物2-(2-Nitro-4-trifluoromethylphenoxy)-4,5-dichlorobenzeneHCID 1343009—

反応条件

温度120 °C

反応手順

A mixture of 3,4-dichlorophenol (25 gram (hereinafter g), 0.153 mol), 4-chloro-3-nitrobenzo-trifluoride (52 g, 0.23 mol) and potassium carbonate (63 g, 0.459 mol) in dimethylformamide (450 mL)was stirred under argon at 120° C. for 24 h. The reaction mixture was filtered and the filtrate evaporated. The residue was dissolved in ethyl acetate, washed with water, brine, dried over anhydrous magnesium sulfate, filtered and evaporated. The residue was flash chromatographed (silica gel, methylene chloride/hexane), to give the title compound as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05470882
出典データセットuspto-grants-1995_11
ORD IDord-2c6a3196267a4fda9525cf2daac82a75
出典メモuspto-grants-1995_11