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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253358Generated: November 4, 2026

1-Butyne → 2-(1-Butynyl)pyridine

https://huagongshe.com/reaction/2253358

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

To a solution of 2-bromopyridine (50 g) dissolved in diethylamine (500 mL) was added dichlorobis(triphenylphosphine)palladium(II) (2.2 g) and copper iodide (0.3 g), and the reaction mixture was stirred for 4 hours at room temperature while introducing 1-butyne (100 g) as a gas. The resulting reaction mixture was bubbled with nitrogen, and then ethyl acetate was added. After the reaction mixture was filtered through celite to remove insoluble residue, the filtrate was washed with water and brine. The obtained organic extract was dried over anhydrous magnesium sulfate and filtered, the solvent was evaporated under reduced pressure, the residue was purified by silica gel column chromatography and the title compound (35 g) was obtained as a brown oil from the n-hexane:ethyl acetate (5:1) fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323569B2
Source datasetuspto-grants-2008_01
ORD IDord-c90231bd4871418ba21b4f5b6e247ea2
Source noteuspto-grants-2008_01