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HRID 856612作成日:2026年10月27日

Water → (4-Amino-2-trifluoromethylphenyl)(4-methylpyridin-2-yl)methanol

https://huagongshe.com/reaction/856612

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium AzideHCID 33557—
反応物2-(4-Fluoro-2-trifluoromethylbenzoyl)-4-methylpyridineHCID 22938526—
溶媒Dimethyl SulfoxideHCID 679—
生成物(4-Amino-2-trifluoromethylphenyl)(4-methylpyridin-2-yl)methanolHCID 2293851080.3%

反応条件

温度90 °C

反応手順

2-(4-fluoro-2-trifluoromethylbenzoyl)-4-methylpyridine (4.5 g) and sodium azide (1.3 g) were suspended in dimethylsulfoxide (30 ml), and the mixture was heated with stirring overnight under nitrogen atmosphere at 90° C. The mixture was poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and then, the solvent was evaporated. The residue was dissolved in tetrahydrofuran (30 ml), and to the solution was added aluminum lithium hydride (1.2 g) under ice-cooling, and the mixture was stirred for 1 hour under nitrogen atmosphere under ice-cooling. Water (1.2 ml), 15% aqueous solution of sodium hydroxide (1.2 ml) and water (3.6 ml) were added to the mixture, and the mixture was stirred, dried over anhydrous magnesium sulfate, and filtrated. The solvent of the filtrate was distilled off, to give (4-amino-2-trifluoromethylphenyl)(4-methylpyridin-2-yl)methanol (3.6 g) as colorless crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07262185B2
出典データセットuspto-grants-2007_08
ORD IDord-6e182b5deb8b49e48f6c951ea182d770
出典メモuspto-grants-2007_08