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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 919292Generated: November 3, 2026

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

https://huagongshe.com/reaction/919292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant5-Bromo-2-methoxypyridineHCID 2734895—
ReactantHCID 178476685HCID 178476685—
SolventAcetonitrileHCID 6342—
Product5-Bromo-1-methylpyridin-2(1H)-oneHCID 13024027—

Reaction Steps

A mixture of 5-bromo-2-methoxypyridine (1) (500 mg, 2.66 mmol), iodomethane (755 mg, 5.32 mmol) and CH3COOK (782 mg, 7.98 mmol) in acetonitrile (5 mL) was heated at reflux for 18 h. After cooled to rt, the mixture was filtered. The filtrate was concentrated and purified by reverse phase silica gel (MeOH in 0.05% NH3.H2O/H2O 10-95% v/v as mobile phase) to afford 2 as a white solid. ESI-MS: 189.0 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273033B2
Source datasetuspto-grants-2016_03
ORD IDord-c67a19e1d6f4461cacf9a8d8b053132a
Source noteuspto-grants-2016_03