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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478303Generated: November 2, 2026

Methyl iodide → 2-Bromo-4-chloro-3-methoxypyridine

https://huagongshe.com/reaction/1478303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-4-chloropyridin-3-olHCID 72213999—
SolventAcetoneHCID 180—
Product2-Bromo-4-chloro-3-methoxypyridineHCID 8669674378.2%

Reaction Steps

2-bromo-4-chloropyridin-3-ol (8.15 g, 39.1 mmol), potassium carbonate (10.5 g, 76 mmol) and iodomethane (3.65 ml, 58.6 mmol) were added to acetone (300 ml) and stirred for 18 h at room temperature under inert conditions. The reaction mixture was evaporated to dryness, dissolved in ethyl acetate (100 mL), filtered over silica gel and the filter washed with ethyl acetate (3×100 mL). The filtrate was evaporated to dryness to obtain crude product which was purified over silica gel using 0:1 to 1:0 ethyl acetate in heptane to obtain 2-bromo-4-chloro-3-methoxypyridine as a white crystalline solid (6.8 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403818B2
Source datasetuspto-grants-2016_08
ORD IDord-6faca156b82f4634ab39fe7216bb9805
Source noteuspto-grants-2016_08