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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48505Generated: October 27, 2026

Methyl iodide → 3-Bromo-2-methoxypyridine

https://huagongshe.com/reaction/48505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 178517701HCID 178517701—
CatalystHCID 178418647HCID 178418647—
SolventBenzeneHCID 241—
Product3-Bromo-2-methoxypyridineHCID 1253339062.5%

Reaction Steps

Under an argon atmosphere, a mixture of 3-bromo-2-hydroxypyridine (3.49 g, 20 mmol), silver carbonate (3.67 g, 13.31 mmol), and iodomethane (1.5 mL, 24.1 mmol) in benzene (30 mL) was stirred in the dark at 40° C. to 50° C. for 24 hours, cooled in an ice bath, and filtered. The filtrate was washed once with 2% aqueous sodium bicarbonate and twice with water, dried (MgSO4), the benzene was evaporated at atmospheric pressure, and the residue was purified by flash chromatography (eluting with hexane/ethyl acetate, 2:1) to obtain the title compound (2.35 g, 12.5 mmol, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06703502B2
Source datasetuspto-grants-2004_03
ORD IDord-8491b1544a2849a8b98bcf685ae424b5
Source noteuspto-grants-2004_03