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HRID 16474作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物4-FluorobenzaldehydeHCID 68023—
反応物Sodium BicarbonateHCID 516892—
反応物4-(Oxazol-2-yl)phenolHCID 135621459—
溶媒DimethylformamideHCID 6228—
生成物4-(4-(2-Oxazolyl)phenoxy)benzaldehydeHCID 8661343894.8%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737145B2
出典データセットuspto-grants-2010_06
ORD IDord-459bf0305e284beaae1e3ca5b5ccc755
出典メモuspto-grants-2010_06