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HRID 606834Erstellt: 24. Oktober 2026

Triethylamine → 5-(2-Chlorophenylethynyl)-nicotinonitrile

https://huagongshe.com/de/reaction/606834

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-Chloro-2-iodobenzeneHCID 11993—
Edukt5-EthynylnicotinonitrileHCID 22416563—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178419050HCID 178419050—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-(2-Chlorophenylethynyl)-nicotinonitrileHCID 67047628—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

Add bis(triphenylphosphine)palladium (II) dichloride (63.2 mg, 0.090 mmol), copper (I) iodide (34.3 mg, 0.180 mmol), and 5-ethynylnicotinonitrile (242 mg, 1.89 mmol), (prepared essentially as described in PREPARATION 4), to a solution of 1-chloro-2-iodobenzene (0.22 mL, 1.77 mmol) in triethylamine (3.60 mL, 25.8 mmol) and heat to 70° C. in a sealed tube for 1.5 h. Cool to room temperature and dilute with ethyl acetate. Wash with a saturated aqueous solution of sodium chloride, dry (sodium sulfate), filter and concentrate. Purify the residue by silica gel chromatography, eluting with a gradient from 95:5 to 80:20 (90:10 hexanes:ethyl acetate):dichloromethane, to give the title compound as a yellow solid. Further purify the title compound by recrystallizing from cyclohexane (20 mL) to give a white solid (95 mg, 22%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07915424B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-472f3e7c898b4541addc1898ad687706
Quellennotizuspto-grants-2011_03