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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948870Generated: October 30, 2026

Methyl iodide → 2-Bromo-3-methoxypyridine

https://huagongshe.com/reaction/1948870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-Bromo-3-pyridinolHCID 23070—
ReactantSodium methanolate methanolHCID 23694274—
SolventDimethyl SulfoxideHCID 679—
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 1 mol/L sodium methoxide-methanol solution 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, and then 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. After the solvent was distilled off under reduced pressure, 65.4 g (corresponding to 0.348 mol) of 2-bromo-3-methoxypyridine was obtained (FIG. 3, Step 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399672B2
Source datasetuspto-grants-2013_03
ORD IDord-e69de426450c4d2da0db02313b424fff
Source noteuspto-grants-2013_03