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HRID 586320作成日:2026年10月25日

Potassium Carbonate → 4-Fluoro-3-(pyridin-3-yl)aniline

https://huagongshe.com/reaction/586320

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3-(Diethylboryl)pyridineHCID 642851—
反応物3-Bromo-4-fluoroanilineHCID 2779286—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物4-Fluoro-3-(pyridin-3-yl)anilineHCID 2228533046.4%

反応条件

温度80 °C

反応手順

A mixture of 3-bromo-4-fluorophenylamine (7.92 g, 41.7 mmol), diethyl(3-pyridyl)borane (6.74 g, 45.9 mmol), tetrakis(triphenylphosphine)palladium(0) (0.96 g, 0.83 mmol) and potassium carbonate (17.26 g, 125 mmol) in 1,2-dimethoxyethane (30 ml) and water (15 ml) was heated at 80° C. for 20 h. After cooling to ambient temperature the reaction was partitioned between ethyl acetate (500 ml) and water (500 ml). The organics were washed with brine (400 ml), dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. Purification of the residue by flash chromatography (silica gel, 0-20% EtOAc/CH2Cl2) gave 4-fluoro-3-(pyridin-3-yl)phenylamine (3.64 g, 46%) as a colourless oil that solidified on standing to afford a white solid: 1H NMR (360 MHz, CDCl3) δ 3.65 (2H, s), 6.65-6.72 (2H, m), 6.99 (1H, dd, J 9, 9 Hz), 7.33-7.37 (1H, m), 7.84-7.86 (1H, m), 8.58 (1H, d, J 4 Hz), 8.76 (1H, m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06936608B2
出典データセットuspto-grants-2005_08
ORD IDord-466660e338dd478299cb5271e67e8627
出典メモuspto-grants-2005_08