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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109774Generated: October 30, 2026

Dimethylformamide → 5-Bromo-2-iodo-3-methoxypyridine

https://huagongshe.com/reaction/2109774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant5-Bromo-2-iodopyridin-3-olHCID 22602985—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
Product5-Bromo-2-iodo-3-methoxypyridineHCID 2422921178.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 5-bromo-2-iodopyridin-3-ol (2.17 g, 7.2 mmol) in DMF (10.00 mL, 129 mmol) was added NaH (0.32 g, 8.0 mmol) at 0° C. The resulting mixture was stirred at 0° C. and MeI was added at 0° C. The resulting mixture was stirred at room temperature for 2 hours. The reaction mixture was diluted with NH4Cl(aq) and water (10 mL each) at 0° C., and diluted with EtOAc (15 mL). The separated aqueous layer was extracted with EtOAc (2×15 mL) and the combined organic layers were washed with water and saturated sodium chloride, dried over Na2SO4, and concentrated to give the crude residue which was purified with flash column chromatography ((5%→50% EtOAc in hexane) to obtain 5-bromo-2-iodo-3-methoxypyridine as an off-white solid (1.77 g, 78% yield) m/z (%): 314.2 (100%, M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514566B2
Source datasetuspto-grants-2009_04
ORD IDord-39d08b197d964df88455866ee031fcb9
Source noteuspto-grants-2009_04