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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 71087Erstellt: 23. Oktober 2026

Acetonitrile → 5-(4-Bromo-2-fluorophenyl)-2-methyloxazole

https://huagongshe.com/de/reaction/71087

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrileHCID 6342—
EduktTrifluoromethanesulfonic acidHCID 62406—
EduktSodium BicarbonateHCID 516892—
EduktIodo benzene diacetateHCID 12217721—
Edukt1-(4-Bromo-2-fluorophenyl)ethan-1-oneHCID 21938581—
Produkt5-(4-Bromo-2-fluorophenyl)-2-methyloxazoleHCID 66608226—

Reaktionsschritte

To a suspension of iodobenzene diacetate (6.7 g) in acetonitrile (100 mL) was added dropwise trifluoromethanesulfonic acid (3.7 mL), and the mixture was stirred at room temperature for 30 min. A mixture of 1-(4-bromo-2-fluorophenyl)ethanone (6.7 g) in acetonitrile (20 mL) was added to the reaction mixture, and the mixture was heated under reflux for 2 hr. The reaction mixture was allowed to cool to room temperature, and neutralized with saturated aqueous sodium hydrogen carbonate solution, and the solvent was evaporated under reduced pressure. The residue was extracted with ethyl acetate, the extract was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (2.6 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822699B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-a5e7c4b700384101bf871aa4d6851407
Quellennotizuspto-grants-2014_09