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HRID 1432874作成日:2026年10月27日

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

https://huagongshe.com/reaction/1432874

反応式

関与物質

役割名称HCID仕込み量
反応物2-Bromo-5-iodo-3-methylpyridineHCID 10108680—
反応物Sodium MethoxideHCID 10942334—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物5-Iodo-2-methoxy-3-methylpyridineHCID 5341599071.8%

反応手順

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+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07612075B2
出典データセットuspto-grants-2009_11
ORD IDord-1e6d615f5fbe42699a7390bfa217cf1d
出典メモuspto-grants-2009_11