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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1432874생성일: 2026년 10월 27일

2-Bromo-5-iodo-3-methylpyridine → 5-Iodo-2-methoxy-3-methylpyridine

https://huagongshe.com/reaction/1432874

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-5-iodo-3-methylpyridineHCID 10108680—
반응물Sodium MethoxideHCID 10942334—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물5-Iodo-2-methoxy-3-methylpyridineHCID 5341599071.8%

반응 단계

To a solution containing 2-bromo-5-iodo-3-methyl-pyridine (4.80 g, 16.0 mmol) in DMSO (15 mL) is added methanolic NaOMe (3.33 M, 5.3 mL, 17.7 mmol) at 0° C. The solution is allowed to warm to ambient temperature and then heated at 70° C. for 1 hour. The reaction mixture is diluted with diethyl ether (300 mL) and water (200 mL) and the layers are separated. The organic phase is washed with brine, dried over anhydrous Na2SO4, filtered and concentrated. The crude product is purified by silica gel flash column chromatography (hexane/diethyl ether, 19:1) to provide 2.86 g (71%) of the title compound as a white solid. 1H NMR (300 MHz, CDCl3) δ2.12 (s, 3H), 3.90 (s, 3H), 7.60 (d, J=2.1 Hz, 1H), 8.14 (d, J=2.1 Hz, 1H) ppm; MS (EI): m/z 249 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07612075B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-1e6d615f5fbe42699a7390bfa217cf1d
출처 메모uspto-grants-2009_11