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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9178Generated: October 23, 2026

1-Butyne → 2-(1-Butynyl)pyridine

https://huagongshe.com/en/reaction/9178

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButyneHCID 7846—
Reactant2-BromopyridineHCID 7973—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventDiethylamineHCID 8021—
Product2-(1-Butynyl)pyridineHCID 2129939184.3%

Reaction Steps

After dissolving 2-bromopyridine (50 g) in diethylamine (500 mL) and adding dichlorobis(triphenylphosphine)palladium (II) (2.2 g) and copper iodide (0.3 g), the mixture was stirred at room temperature for 4 hours while introducing 1-butyne (100 g) as a gas. After bubbling in nitrogen, extraction was performed with ethyl acetate. The insoluble portion was filtered out with celite, and then the organic layer was washed with water and brine. After drying over anhydrous magnesium sulfate and filtration, the solvent was concentrated under reduced pressure, the residue was purified by silica gel column chromatography, and the title compound (35 g) was obtained from the n-hexane:ethyl acetate (5:1) fraction as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091215B2
Source datasetuspto-grants-2006_08
ORD IDord-59f92c1ad5ac44d88c3cda7c11cfe96d
Source noteuspto-grants-2006_08