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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 606838Erstellt: 25. Oktober 2026

Triethylamine → 5-(3,4-Dimethylphenylethynyl)-nicotinonitrile

https://huagongshe.com/reaction/606838

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt4-Iodo-1,2-dimethylbenzeneHCID 141646—
Edukt5-EthynylnicotinonitrileHCID 22416563—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178419050HCID 178419050—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelAcetonitrileHCID 6342—
Produkt5-(3,4-Dimethylphenylethynyl)-nicotinonitrileHCID 6704754262%

Reaktionsschritte

Combine 4-iodo-o-xylene (0.362 g, 1.561 mmol), bis(triphenylphosphine)palladium (II) dichloride (55 mg, 0.078 mmol), and copper (I) iodide (30 mg, 0.156 mmol) in triethylamine (0.653 mL, 4.683 mmol) and stir under nitrogen for 5 min at 80° C. Add a solution of 5-ethynylnicotinonitrile, (prepared essentially as described in PREPARATION 4), (200 mg, 1.561 mmol) in anhydrous acetonitrile (2.50 mL), and stir under nitrogen overnight. Cool to room temperature and dilute with diethyl ether. Wash with a saturated aqueous solution of sodium bicarbonate, dry (sodium sulfate), filter, and concentrate. Purify the residue by silica gel chromatography, eluting with 95:5 to 50:50 dichloromethane:ethyl acetate, to give the title compound as a yellow solid (225 mg, 62%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07915424B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-f070616815b445c8816ea82e3b9c3f6a
Quellennotizuspto-grants-2011_03