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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513696Generated: November 3, 2026

Methyl iodide → 5-Bromo-1-methylpyridin-2(1H)-one

https://huagongshe.com/reaction/1513696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-hydroxypyridineHCID 599528—
SolventDimethylformamideHCID 6228—
Product5-Bromo-1-methylpyridin-2(1H)-oneHCID 13024027—

Reaction Steps

5-Bromopyridin-2(1H)-one (0.250 g, 1.44 mmol) was dissolved in DMF (3 mL) then added iodomethane (0.0943 ml, 1.51 mmol) and potassium carbonate (0.218 g, 1.58 mmol). The reaction was stirred at room temperature overnight. The reaction mixture was concentrated under vacuum. The remaining residue was dissolved in ethyl acetate then washed with water and brine. The aqueous layer was back-extracted with ethyl acetate (3×). The organic layers were combined and dried over sodium sulfate then concentrated under vacuum to afford 5-bromo-1-methylpyridin-2(1H)-one as an orange waxy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217177B2
Source datasetuspto-grants-2012_07
ORD IDord-6341040decc24f0ea80da3660d454116
Source noteuspto-grants-2012_07