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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473743Generated: October 26, 2026

Methyl iodide → 3-Bromo-2-chloro-5-methoxypyridine

https://huagongshe.com/reaction/473743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-6-chloropyridin-3-olHCID 14595226—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-Bromo-2-chloro-5-methoxypyridineHCID 46738814—

Reaction Steps

To a stirred mixture of 5-bromo-6-chloropyridin-3-ol (2.95 g, 14.15 mmol) and potassium carbonate (1.28 mL, 21.23 mmol) in acetonitrile (45 mL) under a nitrogen atmosphere was added iodomethane (0.93 mL, 14.86 mmol). The reaction mixture was stirred at room temperature for 24 h. The reaction mixture was diluted with water and extracted with EtOAc (2×). The combined organic layers were washed with sat. sodium chloride, dried over magnesium sulfate, filtered, and concentrated. The resulting crude product was purified by silica gel chromatography to give 3-bromo-2-chloro-5-methoxypyridine. MS (ESI, pos. ion) m/z: 221.9 and 223.9 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637500B2
Source datasetuspto-grants-2014_01
ORD IDord-955f172ddda64ad9983685d692155e5b
Source noteuspto-grants-2014_01