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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 606928Erstellt: 24. Oktober 2026

1-Fluoro-3-iodobenzene → 5-(3-Fluorophenylethynyl)-nicotinic acid ethyl ester

https://huagongshe.com/de/reaction/606928

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Fluoro-3-iodobenzeneHCID 70725—
EduktTetrabutylammonium FluorideHCID 2724141—
EduktEthyl 5-((trimethylsilyl)ethynyl)nicotinateHCID 67047749—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178419050HCID 178419050—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-(3-Fluorophenylethynyl)-nicotinic acid ethyl esterHCID 6704776280%

Reaktionsschritte

Add a 1 M solution of tetrabutylammonium fluoride (0.88 g, 3.38 mmol) in tetrahydrofuran to a mixture of 3-iodofluorobenzene (0.50 g, 2.25 mmol), 5-trimethylsilanylethynyl-nicotinic acid ethyl ester, (prepared as described in PREPARATION 16), (0.84 g, 3.38 mmol), bis(triphenylphosphine)palladium (II) dichloride (0.03 g, 0.05 mmol) and copper (I) iodide (0.02 g, 0.09 mmol) at −78° C. Warm to room temperature, stir overnight and then dilute with ethyl acetate. Wash with an aqueous saturated solution of ammonium chloride, dry (magnesium sulfate), filter and concentrate. Purify the residue by silica gel chromatography, eluting with 2.5:45:52.5 ethyl acetate:chloroform:hexanes, to give the title compound as a pale yellow solid (0.46 mg, 80%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07915424B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-1237bf71b2dd440cace619e612230c93
Quellennotizuspto-grants-2011_03