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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 235181Erstellt: 25. Oktober 2026

Tetrahydrofuran → 2-(1-Undecynyl)fluorobenzene

https://huagongshe.com/reaction/235181

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktTriethylamineHCID 8471—
Edukt1-Bromo-2-fluorobenzeneHCID 61259—
Edukt1-UndecyneHCID 75249—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(1-Undecynyl)fluorobenzeneHCID 1837302153,2%

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

To a solution of 2-bromofluorobenzene (17.5 g), 1-undecyne (18.3 g), tetrahydrofuran (50 ml), and triethylamine (70 ml) was added bistriphenylphosphine palladium(II)chloride (1.2 g) and copper(I) iodide (162 mg). The reaction mixture was stirred at 55° C. for 3 hr, and an additional 2-bromofluorobenzene (2.0 g) and bistriphenylphosphine palladium(II)chloride (200 mg) were added. The mixture was stirred at 55° C. overnight, allowed to cool to room temperature, diluted with ethyl acetate and washed with water. The organic phase was dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated in vacuo. The residue was chromatographed over silica gel (eluted with hexane). The appropriate fractions were collected and evaporated. The residue was distilled twice under vacuum to give 13.1 g (53%) of product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05597838
Quelldatensatzuspto-grants-1997_01
ORD IDord-c57da39cfede4c2aa93d3082f6ede134
Quellennotizuspto-grants-1997_01