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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1626Erstellt: 23. Oktober 2026

Triethylamine → 4-[(5-Nitro-furan-2-yl)-ethynyl]benzonitrile

https://huagongshe.com/de/reaction/1626

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-Bromo-5-nitrofuranHCID 233582—
Edukt4-EthynylbenzonitrileHCID 4547245—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelAcetonitrileHCID 6342—
Produkt4-[(5-Nitro-furan-2-yl)-ethynyl]benzonitrileHCID 19691951—

Reaktionsschritte

To a solution of 2-bromo-5-nitrofuran (1.65 g) and triethylamine (34 ml) in anhydrous acetonitrile (55 ml) under nitrogen was added bis(triphenylphosphine)palladium dichloride (130 mg) and cuprous iodide (35 mg). 4-Ethynylbenzonitrile (1.09 g) was added and the reaction mixture was stirred under nitrogen overnight. The mixture was evaporated to dryness and the residue was dissolved in dichloromethane (200 ml), dried over anhydrous sodium sulfate, filtered and evaporated to dryness. The residue was purified by silica gel chromatography (ethyl acetate/hexane 1:10) and triturated with ethyl acetate/hexane (1:3) to give 4-[(5-nitro-2-furyl)-ethynyl]benzonitrile.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726195
Quelldatensatzuspto-grants-1998_03
ORD IDord-fd2ce529eb5e4230a968d9b7a9207cfc
Quellennotizuspto-grants-1998_03