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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910635Generated: November 2, 2026

Methyl iodide → 2-Bromo-3-methoxypyridine

https://huagongshe.com/reaction/910635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-Bromo-3-pyridinolHCID 23070—
ReactantSodium methanolate methanolHCID 23694274—
SolventDimethyl SulfoxideHCID 679—
Product2-Bromo-3-methoxypyridineHCID 90364122.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

31.11 g (corresponding to 178.88 mmol) of 2-bromo-3-hydroxypyridine was dissolved in 95.8 mL of dimethylsulfoxide, and 89.9 mL (corresponding to 89.9 mmol) of 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 5° C. or lower, 29.2 g (corresponding to 205.62 mmol) of methyl iodide was added, and then stirred at room temperature for 17 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 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, 20.74 g (corresponding to 110.31 mmol) of 2-bromo-3-methoxypyridine was obtained (FIG. 5, Step 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022207B2
Source datasetuspto-grants-2011_09
ORD IDord-648d5e2b88344235b86d9c4b59446c35
Source noteuspto-grants-2011_09