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HRID 77724作成日:2026年10月27日

Toluene → 6-methyl-3'-nitro-N-[3-(trifluoromethyl)phenyl]biphenyl-3-carboxamide

https://huagongshe.com/reaction/77724

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Potassium CarbonateHCID 11430—
反応物3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)nitrobenzeneHCID 11265164—
反応物3-iodo-4-methyl-N-(3-(trifluoromethyl)phenyl)benzamideHCID 17197569—
触媒HCID 178418397HCID 178418397—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物6-methyl-3'-nitro-N-[3-(trifluoromethyl)phenyl]biphenyl-3-carboxamideHCID 69273781—

反応手順

4,4,5,5-Tetramethyl-2-(3-nitrophenyl)-1,3,2-dioxaborolane (1.4 g, 5.6 mmol) was mixed with 3-iodo-4-methyl-N-[3-(trifluoromethyl)phenyl]benzamide (2.00 g, 4.94 mmol), potassium carbonate (1.4 g, 9.9 mmol), toluene (40 mL), ethanol (6.0 mL), and water (4.0 mL). The mixture was degassed and tetrakis(triphenylphosphine)palladium(0) (0.27 g, 0.24 mmol) was added. The resulting mixture was heated to reflux for 16 hours. The reaction was then cooled and was extracted with ethyl acetate. The organic extracts were washed with water, brine, dried (Na2SO4) and concentrated. The product was purified by flash column chromatography, eluting with a gradient of 20-50% ethyl acetate in hexanes (1.92 g, 91%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841318B2
出典データセットuspto-grants-2014_09
ORD IDord-4b33ffaa42fa4924988fa781d468829c
出典メモuspto-grants-2014_09