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HRID 410176作成日:2026年10月25日

4-Aminophenol → 4-[(3-methyl-2-pyridinyl)oxy]Benzenamine

https://huagongshe.com/reaction/410176

反応式

関与物質

役割名称HCID仕込み量
反応物4-AminophenolHCID 403—
反応物Cesium carbonateHCID 10796—
反応物2-Fluoro-3-methylpyridineHCID 242722—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Ethyl AcetateHCID 8857—
生成物4-[(3-methyl-2-pyridinyl)oxy]BenzenamineHCID 59326808—

反応条件

温度80 °C

反応手順

To a solution of 4-aminophenol (0.87 g, 8.0 mmol) in DMSO (12 mL) was added cesium carbonate (3.1 g, 9.6 mmol) and 2-fluoro-3-picoline (0.89 g, 8.0 mmol). The resulting mixture was heated to 80° C. for 16 h. After cooling to RT, the reaction mixture was diluted with EtOAc and washed with water and brine several times to remove DMSO. The aqueous layer was back extracted with EtOAc and the combined organic layer was dried (Na2SO4) and concentrated. The crude product was chromatographed through a RediSep® pre-packed silica gel column (120 g), eluting with a gradient of 0% to 30% EtOAc in hexane, to provide 4-(3-methylpyridin-2-yloxy)benzenamine as tan solid. MS (ESI, pos. ion) m/z: 201.2 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08759532B2
出典データセットuspto-grants-2014_06
ORD IDord-8e3643de866e4aaab94d37818fd64280
出典メモuspto-grants-2014_06