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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 525998생성일: 2026년 10월 26일

Iodopentafluoroethane → 5-(Perfluoroethyl)pyridin-2-amine

https://huagongshe.com/reaction/525998

반응식

참여 물질

역할이름HCID투입량
반응물IodopentafluoroethaneHCID 9636—
반응물2-AminopyridineHCID 10439—
반응물Sodium DithioniteHCID 24489—
반응물Sodium BicarbonateHCID 516892—
촉매Tetrabutylammonium hydrogen sulfateHCID 94433—
용매WaterHCID 962—
용매tert-Butyl methyl etherHCID 15413—
생성물5-(Perfluoroethyl)pyridin-2-amineHCID 498535557%

반응 단계

To a solution of 2-aminopyridine (25.0 g, 263 mmol) in a mixture of water (250 ml) and tert-butyl methyl ether (25 ml) was added, successively perfluoroethyl iodide (80 g, 38 ml, 315 mmol), sodium hydrosulfite (64.6 g, 26 ml, 315 mmol), sodium hydrogen carbonate (26.5 g, 315.6 mmol) and tetrabutyl ammonium hydrogen sulfate (“TBAHS”) (0.11 equiv., 9.92 g, 28.9 mmol). The reaction mixture was stirred at ambient temperature for 16 h. The mixture was filtered and the filtrate was extracted twice with tert-butyl methyl ether. The combined organic phases were washed successively with water, aqueous hydrochloric acid (1N) and brine, dried over sodium sulfate and concentrated. The residue was purified by flash chromatography (AcOEt/cyclohexane) to give 5-(1,1,2,2,2-pentafluoroethyl)pyridin-2-amine in 7% yield. 1H NMR (400 MHz, CDCl3) 8.23 (d, 1H), 7.61 (d, 1H), 6.72 (m, 1H), 5.04 (sb, 2H, NH2) ppm. The major by-product was 3,5-bis(1,1,2,2,2-pentafluoroethyl)pyridin-2-amine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09345244B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-de29af16b93140d58208adafbb6ed116
출처 메모uspto-grants-2016_05