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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20330Erstellt: 23. Oktober 2026

Vinyl Acetate → 1-Fluoro-2-(2-vinyloxyethyl)-benzene

https://huagongshe.com/de/reaction/20330

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktVinyl AcetateHCID 7904—
EduktSodium CarbonateHCID 10340—
Edukt2-(2-Fluorophenyl)ethan-1-olHCID 2733296—
KatalysatorChloro(1,5-cyclooctadiene)iridium(I) dimerHCID 6436381—
LösungsmittelTolueneHCID 1140—
Produkt1-Fluoro-2-(2-vinyloxyethyl)-benzeneHCID 6856353272,2%

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

Combine 2-(2-fluorophenyl)-ethanol (3.08 g, 22.0 mmol), vinyl acetate (4 mL, 43.3 mmol), anhydrous toluene (22 mL), chloro(1,5-cyclooctadiene)iridium(I) dimer (155 mg, 0.231 mmol), and anhydrous sodium carbonate (1.5 g, 14.2 mmol) in a dry round-bottom flask fitted with a reflux condensor under a nitrogen atmosphere. Heat the resulting mixture to 95° C. for 5 hours. Cool the reaction mixture to room temperature. Vacuum filter the resultant slurry to remove inorganic precipitates, washing the collected solid with hexanes. Concentrate and purify (silica gel chromatography, eluting with hexanes) to give the title compound as a yellow oil (2.64 g, 72%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745438B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-7b1b0cb0cdd642c8a96a6098f2f2bb17
Quellennotizuspto-grants-2010_06