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HRID 1826833作成日:2026年10月27日

Phenol → 2-Phenoxy-6-(phenylamino)benzonitrile

https://huagongshe.com/reaction/1826833

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物Sodium hydrideHCID 24758—
反応物Phenolate SodiumHCID 4445035—
反応物2-Fluoro-6-(phenylamino)benzonitrileHCID 13469799—
溶媒Dimethyl SulfoxideHCID 679—
溶媒TetrahydrofuranHCID 8028—
生成物2-Phenoxy-6-(phenylamino)benzonitrileHCID 22136226—

反応条件

温度110 °C

反応手順

Sodium phenoxide was generated by dissolving phenol (0.36 g, 3.83 mmol) in dry tetrahydrofuran (5 mL), and adding sodium hydride (0.087 g, 3.6 mmol). After gas evolution ceased, the solvent was evaporated and 2-fluoro-6-(phenylamino)benzonitrile (0.6 g, 2.83 mmol) dissolved in dimethyl sulfoxide (10 mL) was added. The mixture was heated to 110° C. while stirring under argon for 4 hours. The solvent was evaporated in vacuo, and the residue was partitioned between ethyl acetate and water. The organic phase was washed with water (5×), brine (1×) dried over anhydrous Na2SO4 filtered, and evaporated to give the crude product which was then chromatographed on silica gel eluted with 10–40% CH2Cl2 in hexane to give the title compound as a white amorphous solid. mp 146–147° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07053099B1
出典データセットuspto-grants-2006_05
ORD IDord-a88a8d277a694ee585d5cae87833e4f4
出典メモuspto-grants-2006_05