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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16474생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-FluorobenzaldehydeHCID 68023—
반응물Sodium BicarbonateHCID 516892—
반응물4-(Oxazol-2-yl)phenolHCID 135621459—
용매DimethylformamideHCID 6228—
생성물4-(4-(2-Oxazolyl)phenoxy)benzaldehydeHCID 8661343894.8%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737145B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-459bf0305e284beaae1e3ca5b5ccc755
출처 메모uspto-grants-2010_06