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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181863Generated: November 1, 2026

1-Butyne → 2-(1-Butynyl)-4-methoxypyridine

https://huagongshe.com/reaction/1181863

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButyneHCID 7846—
ReactantDiethylamineHCID 8021—
Reactant2-Bromo-3-methoxypyridineHCID 90364—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
Product2-(1-Butynyl)-4-methoxypyridineHCID 21984661—

Reaction Steps

After adding dichlorobis(triphenylphosphine)palladium (II) (671 mg) and copper iodide (91 mg) to a solution of 2-bromo-3-methoxypyridine (18.0 g) in diethylamine (250 mL), 1-butyne (15.5 g) was bubbled through at room temperature, and the mixture was stirred for 20 hours. Upon completion of the reaction, the solvent was distilled off under reduced pressure. Water was added to the obtained residue, extraction was performed with ethyl acetate, the extract was washed with brine and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was subjected to silica gel column chromatography (500 g), and 2-(1-butynyl)-4-methoxypyridine (10.0 g) was obtained from the n-hexane:ethyl acetate (2:1) fraction as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285666B2
Source datasetuspto-grants-2007_10
ORD IDord-f48f1f37117243eeb48260bf5607ab10
Source noteuspto-grants-2007_10