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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 242412생성일: 2026년 10월 27일

Iodine → 2-Fluoro-3-iodo-5-methylpyridine

https://huagongshe.com/reaction/242412

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물DiisopropylamineHCID 7912—
반응물Sodium ThiosulfateHCID 24477—
반응물2-Fluoro-5-methylpyridineHCID 2774635—
반응물ButyllithiumHCID 178418339—
반응물HCID 178506721HCID 178506721—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2-Fluoro-3-iodo-5-methylpyridineHCID 1024322033.4%

반응 단계

26.5 ml of n-butyllithium (1.57 mol/l hexane solution) was dropwise added at −78° C. to a solution having 4.02 g (39.8 mmol) of diisopropylamine dissolved in 70 ml of tetrahydrofuran, followed by stirring for 30 minutes. To this solution, a solution having 4.42 g (39.8 mmol) of 2-fluoro-5-methylpyridine dissolved in 18 ml of tetrahydrofuran was added, followed by stirring for 4 hours to prepare 2-fluoro-5-methyl-3-pyridyllithium. Then, to this solution, a solution having 10.1 g (39.8 mmol) of iodine dissolved in 27 ml of tetrahydrofuran was added, followed by stirring for 2 hours. 16 ml of water and 120 ml of a sodium thiosulfate aqueous solution were charged, followed by extraction with ethyl ether. The organic layer was dried over magnesium sulfate and subjected to filtration, the solvent was distilled off under reduced pressure, and the obtained crude product was purified by silica gel chromatography to obtain 3.15 g (yield: 33%) of 2-fluoro-3-iodo-5-methylpyridine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653113B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-22aed9edcfd2428bac852decb36eaea7
출처 메모uspto-grants-2014_02