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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037672Generated: October 31, 2026

Methyl iodide → 2-Bromo-3-methoxypyridine

https://huagongshe.com/reaction/1037672

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 numberUS08546581B2
Source datasetuspto-grants-2013_10
ORD IDord-f6e561a818af4b58a5d4d01570673560
Source noteuspto-grants-2013_10