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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77656생성일: 2026년 10월 24일

Acetone → 1,5-Bis(3-fluorophenyl)-1,4-pentadien-3-one

https://huagongshe.com/ko/reaction/77656

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물WaterHCID 962—
반응물Sodium HydroxideHCID 14798—
반응물3-FluorobenzaldehydeHCID 68009—
용매EthanolHCID 702—
생성물1,5-Bis(3-fluorophenyl)-1,4-pentadien-3-oneHCID 6950172242%

반응 단계

3-Fluorobenzaldehyde (1s, 0.5 ml, 4.7 mmol) and acetone (19, 0.18 ml, 2.3 mmol) were combined in ethanol (20 ml) and stirred for 10 min at room temperature. A solution of sodium hydroxide (0.29 g, 7.3 mmol) and water (15 ml) was added and the mixture stirred for 18 hr at room temperature. The resulting mixture was filtered and chromatographed on silica gel with ethyl acetate/hexane to give a solid. The crude was recrystallized from ethanol to afford 0.26 g (42%) of yellow crystals: mp 96-97° C. [expected mp 96-97° C.]; 1H NMR: δ 7.03 (d, 2H, J=16.1 Hz), 7.09 (m, 2H), 7.35 (m, 6H), 7.67 (d, 2H, J=15.9 Hz); 13C NMR: δ 114.4, 117.5, 124.4, 126.3, 130.4, 136.9, 142.0, 162.9, 188.1; Anal. Calcd for C17H12OF2: C, 75.55; H, 4.48. Found: C, 75.26; H, 4.65.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841326B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b896188ea0824f719c74a4f42878ee58
출처 메모uspto-grants-2014_09