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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 235179Erstellt: 26. Oktober 2026

Triethylamine → 2-(1-Dodecynyl)thiophene

https://huagongshe.com/reaction/235179

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-IodothiopheneHCID 18921—
Edukt1-DodecyneHCID 69821—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(1-Dodecynyl)thiopheneHCID 18372993739%

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

To a solution of 2-iodothiophene (31.5 g), 1-dodecyne (2.5 g), triethylamine (105 ml), and tetrahydrofuran (100 ml) was added (bis)triphenylphosphine palladium(II)chloride (1.73 g) followed by copper(I)iodide (0.24 g). The reaction mixture was warmed to 55° C. and stirred for 7 hr. The solution was allowed to cool to room temperature and stirred overnight. The mixture was filtered, and the precipitate was washed with ethyl acetate. The filtrate was diluted with ethyl acetate and washed with water and brine. The organic phase was separated, dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated in vacuo. The residue was flash chromatographed over silica gel (elated with hexane). The appropriate fractions were collected and evaporated. The residue was distilled to afford 27.6 g (74%) of product, bp 145°-150° C. at 0.7 mm Hg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05597838
Quelldatensatzuspto-grants-1997_01
ORD IDord-a5c356321837494d8c050da15a5dc5c6
Quellennotizuspto-grants-1997_01