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HRID 367052作成日:2026年10月26日

Acetonitrile → 2-Fluoro-5-nitropyridine

https://huagongshe.com/reaction/367052

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物2-Chloro-5-nitropyridineHCID 78308—
反応物Potassium FluorideHCID 522689—
触媒Tetraphenylphosphonium BromideHCID 2724163—
溶媒Diethyl EtherHCID 3283—
生成物2-Fluoro-5-nitropyridineHCID 9526454%

反応手順

2-Chloro-5-nitropyridine (100 g, 0.656 mol, Aldrich), potassium fluoride (84.1 g, 1.45 mol, Aldrich), tetraphenylphosphonium bromide (95.3 g, 0.227 mol, Aldrich), and acetonitrile (1.5 L) were combined and heated at reflux until consumption of the 2-chloro-5-nitropyridine was complete. The volume of the mixture was reduced to 750 mL, diluted with 2 L of ether, filtered and concentrated. The resultant residue was triturated with hot hexane, and the combined hexane extracts were concentrated to give of the title compound (48 g, 54%): 1H NMR (CDCl3, 300 MHz) δ 7.15 (dd, J=3, 6 Hz, 1H), 8.64 (m, 1H), 9.15 (d, J=1.6 Hz, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06133253
出典データセットuspto-grants-2000_10
ORD IDord-15c08ec3a41c4b66a02a81bb36bd2c99
出典メモuspto-grants-2000_10