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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551758Generated: November 4, 2026

Methyl iodide → 2-Bromo-3-methoxypyridine

https://huagongshe.com/reaction/551758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-Bromo-3-pyridinolHCID 23070—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product2-Bromo-3-methoxypyridineHCID 9036483%

Reaction Steps

Add sodium hydride (5.91 g, 147.8 mmol) to a rapidly stirred solution of 2-bromo-3-pyridinol in DMF (anhydrous, 200 mL). After 30 minutes, add iodomethane (9.2 mL, 147.8 mmol) and stir under N2 for 2.5 hours. Quench with water and concentrate. Partition residue between Et2O) and water, separate layers. Extract from aqueous layer with Et2O (×2), dry combined layers over MgSO4 and concentrate. Purify residue by flash chromatography on silica gel eluting with 0-25% EtOAc/hexanes to afford 2-bromo-3-methoxy-pyridine (21.0 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947841B2
Source datasetuspto-grants-2011_05
ORD IDord-3e2e9165a2fb4e8a94bdfda89ce7a5bb
Source noteuspto-grants-2011_05