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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 440398Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/440398

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-UndecyneHCID 75249—
Edukt6-Bromopyridine-2-carbaldehydeHCID 2757009—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorDichlorobis(triphenylphosphine)palladiumHCID 6102075—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-(1-Undecynyl)pyridine-2-carboxaldehydeHCID 1538064684,3%

Reaktionsschritte

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 nitorgen 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05519062
Quelldatensatzuspto-grants-1996_05
ORD IDord-e2f508ff91164d89b02ab1303cb8bd09
Quellennotizuspto-grants-1996_05