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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 367052생성일: 2026년 10월 25일

Acetonitrile → 2-Fluoro-5-nitropyridine

https://huagongshe.com/reaction/367052

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물2-Chloro-5-nitropyridineHCID 78308—
반응물Potassium FluorideHCID 522689—
촉매Tetraphenylphosphonium BromideHCID 2724163—
용매Diethyl EtherHCID 3283—
생성물2-Fluoro-5-nitropyridineHCID 9526454%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06133253
출처 데이터셋uspto-grants-2000_10
ORD IDord-15c08ec3a41c4b66a02a81bb36bd2c99
출처 메모uspto-grants-2000_10