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HRID 13637作成日:2026年10月24日

Sodium Hydroxide → Tris(2-bromo-6-pyridyl)fluoromethane

https://huagongshe.com/ja/reaction/13637

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物(Diethylamino)sulfur trifluorideHCID 123472—
反応物Tris(6-bromopyridin-2-yl)methanolHCID 53880796—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Tris(2-bromo-6-pyridyl)fluoromethaneHCID 58036607—

反応条件

温度5 °C

反応手順

A solution of 50.0 g (100 mmol) of tris(2-bromo-6-pyridyl)methanol in 750 ml of dichloromethane was admixed with good stirring dropwise with 47.3 ml (400 mmol) of diethylaminosulfur trifluoride. Subsequently, the reaction mixture was heated under reflux for 30 min, then cooled to 5° C., and admixed with good stirring (highly exothermic!!!) with 300 ml of water and then with a solution of 64.0 g (1600 mmol) of sodium hydroxide in 600 ml of water (highly exothermic!!!). The organic phase was removed, the aqueous phase was washed twice with 200 ml of dichloromethane, and the combined organic phases were dried over calcium chloride and subsequently freed of dichloromethane. The remaining red-brown crystal slurry was taken up in 100 ml of methanol and filtered off. After washing with methanol, the colorless to beige crystals were dried under reduced pressure. The yield was 47.4 g (91.3%) at a purity of greater than 99.0% by 1H NMR.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728137B2
出典データセットuspto-grants-2010_06
ORD IDord-a4921898052e487cb961c314a7687d52
出典メモuspto-grants-2010_06