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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379208Generated: November 2, 2026

Triethylamine → 6-(1-Undecynyl)pyridine-2-carboxaldehyde

https://huagongshe.com/reaction/2379208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-UndecyneHCID 75249—
Reactant6-Bromopyridine-2-carbaldehydeHCID 2757009—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTetrahydrofuranHCID 8028—
Product6-(1-Undecynyl)pyridine-2-carboxaldehydeHCID 1538064684.3%

Reaction Steps

A solution of 6-bromopyridine-2-carboxaldehyde (15.0 g), 1-undecyne (12.9 g), triethylamine (24.5 g), bis(triphenylphosphine)palladium(II)chloride (1.1 g, 2%), and copper(I)iodide (0.15 g, 1%) in dry tetrahydrofuran (60 ml) was heated under nitrogen at 55° C. for 10 hrs. The reaction mixture was filtered, the filter cake was washed with ethyl acetate, and the filtrate was evaporated. The residue was dissolved in ethyl acetate, and the solution was washed with half-saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated. The residue was flash chromatographed on silica gel, eluting with 0%-2%-ethyl acetate:hexane. The appropriate fractions were collected and evaporated to yield 17.5 g (84.0%) of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05360811
Source datasetuspto-grants-1994_11
ORD IDord-e026386c13e54df19788db1aa88736ae
Source noteuspto-grants-1994_11