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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181855Generated: October 26, 2026

1-Butyne → 2-(1-Butynyl)pyridine

https://huagongshe.com/reaction/1181855

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 numberUS07285666B2
Source datasetuspto-grants-2007_10
ORD IDord-457cd82ce59544778e5b01d6a0b20f2d
Source noteuspto-grants-2007_10