Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16474Erstellt: 23. Oktober 2026

Potassium Carbonate → 4-(4-(2-Oxazolyl)phenoxy)benzaldehyde

https://huagongshe.com/de/reaction/16474

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt4-FluorobenzaldehydeHCID 68023—
EduktSodium BicarbonateHCID 516892—
Edukt4-(Oxazol-2-yl)phenolHCID 135621459—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(4-(2-Oxazolyl)phenoxy)benzaldehydeHCID 8661343894,8%

Reaktionsschritte

To a solution of 4-(2-oxazolyl)phenol (4.1 g, 25.44 mmol) in DMF (98 ml), K2CO3 (3.52 g, 25.44 mmol, 1 equiv.) was added. The reaction was stirred at ambient temperature for 30 min. Then, 4-fluorobenzaldehyde (2.73 mL, 25.44 mmol, 1 equiv., Aldrich # 12,837-6) was added and stirring was continued at 150° C. for 4 hours. After cooling, saturated NaHCO3 was added to the reaction mixture. The reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4, and concentrated under reduced pressure. Flashmaster chromatography on 50 g of silica gel using a gradient of 100% hexane→50% hexane+50% ethyl acetate gave 6.4 g of 4-[4-(2-oxazolyl)phenoxy]benzaldehyde still containing 20 mol % DMF. Further drying led to the pure product (6.05 g; 90% th.; 148% pract.); 1H NMR (CDCl3) δ 9.95 (s, 1H), 8.09 (d, 2H), 7.89 (d, 2H), 7.72 (d, 1H), 7.24 (d, 1H), 7.16 (d, 2H), 7.13 (d, 2H) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737145B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-459bf0305e284beaae1e3ca5b5ccc755
Quellennotizuspto-grants-2010_06