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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432874Generated: October 26, 2026

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

https://huagongshe.com/reaction/1432874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-5-iodo-3-methylpyridineHCID 10108680—
ReactantSodium MethoxideHCID 10942334—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product5-Iodo-2-methoxy-3-methylpyridineHCID 5341599071.8%

Reaction Steps

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+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-1e6d615f5fbe42699a7390bfa217cf1d
Source noteuspto-grants-2009_11