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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656235Generated: October 29, 2026

Methyl iodide → 5-Bromo-2-methoxy-3-(3-methoxypropoxy)-pyridine

https://huagongshe.com/reaction/656235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant5-bromo-3-(3-methoxypropoxy)-1H-pyridin-2-oneHCID 23149475—
CatalystHCID 178418647HCID 178418647—
SolventBenzeneHCID 241—
Product5-Bromo-2-methoxy-3-(3-methoxypropoxy)-pyridineHCID 23149492—

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture of 113.26 mmol of 5-bromo-3-(3-methoxypropoxy)-1H-pyridin-2-one, 79.28 mmol of silver carbonate and 158.56 mmol of iodomethane in 230 ml of benzene is stirred at 45° C. with exclusion of light for 24 hours. The reaction mixture is cooled to room temperature, and the silver salts are filtered off. The filtrate is washed with 2% sodium bicarbonate solution and water (2×). The organic phase is dried over sodium sulphate and evaporated. The crude title compound is obtained as a beige oil from the residue and is employed without further purification in the next stage. Rf=0.45 (EtOAc-heptane 1:2); Rt=4.34 (Gradient I).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071651B2
Source datasetuspto-grants-2011_12
ORD IDord-2458b09a853349989fa62fcf49c6f0e3
Source noteuspto-grants-2011_12