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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375916Generated: October 27, 2026

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

https://huagongshe.com/reaction/375916

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-caboxaldehyde (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 (0.15g, 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 numberUS05488061
Source datasetuspto-grants-1996_01
ORD IDord-506d31a0fc7f489c992c5f533552ebbb
Source noteuspto-grants-1996_01