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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16474Generated: October 26, 2026

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

https://huagongshe.com/reaction/16474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Oxazol-2-yl)phenolHCID 135621459—
SolventDimethylformamideHCID 6228—
Product4-(4-(2-Oxazolyl)phenoxy)benzaldehydeHCID 8661343894.8%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737145B2
Source datasetuspto-grants-2010_06
ORD IDord-459bf0305e284beaae1e3ca5b5ccc755
Source noteuspto-grants-2010_06