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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059521Generated: October 28, 2026

Methyl iodide → 2-Bromo-3-methoxypyridine

https://huagongshe.com/reaction/2059521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-Bromo-3-pyridinolHCID 23070—
ReactantSodium MethoxideHCID 10942334—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
Product2-Bromo-3-methoxypyridineHCID 90364—

Reaction Conditions

Temperature90 °C

Reaction Steps

100.0 g (corresponding to 0.575 mol) of 2-bromo-3-hydroxypyridine was dissolved in 310 mL of dimethylsulfoxide, and 575 mL (corresponding to 0.575 mol) of a solution of 1 mol/L sodium methoxide in methanol was added thereto. Then, the reaction solution was heated to 90° C. to distill off methanol. After the reaction solution was cooled down to 10° C. or lower, 93.9 g (corresponding to 0.662 mol) of methyl iodide was added thereto, and the mixture was stirred at room temperature for 20.5 hours. After the completion of the reaction, the reaction solution was poured into ice water and extracted twice with chloroform. The combined chloroform layer was washed with a 1 mol/L sodium hydroxide solution, washed twice with a saturated sodium chloride solution, and dried over anhydrous sodium sulfate. Then, the solvent was distilled off under reduced pressure, to obtain 65.4 g (corresponding to 0.348 mol) of 2-bromo-3-methoxypyridine (FIG. 1, Step 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08277777B2
Source datasetuspto-grants-2012_10
ORD IDord-251122566eb94ae5ad78da5fb790734b
Source noteuspto-grants-2012_10