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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283456Generated: October 31, 2026

Methyl iodide → 5-Bromo-2-methoxypyridine

https://huagongshe.com/reaction/2283456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant5-Bromo-2-hydroxypyridineHCID 599528—
CatalystHCID 178418647HCID 178418647—
SolventBenzeneHCID 241—
Product5-Bromo-2-methoxypyridineHCID 273489574%

Reaction Conditions

Temperature50 °C

Reaction Steps

Silver carbonate (16.0 g, 57.8 mmol) and methyl iodide (6.5 mL, 103 mmol) were sequentially added to a solution of 5-bromopyridin-2(1H)-one (15.0 g, 86.2 mmol) in benzene (225 mL). The mixture was stirred for 16 h at 50° C. After cooling to room temperature, the mixture was filtered through celite and concentrated. Purification by chromatography using 1-5% ethyl acetate in pet ether provided 12 g of the desired compound: 1H NMR (300 MHz, CDCl3) 8.15-8.25 (narrow m, 1H), 7.63 (dd, J=9, 3 Hz, 1H), 6.63 (d, J=9 Hz, 1H), 3.92 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145393B2
Source datasetuspto-grants-2015_09
ORD IDord-06cfe2d755b942019db3ba2b1aff63d2
Source noteuspto-grants-2015_09