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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77658생성일: 2026년 10월 23일

Acetone → 1,5-Bis(2-trifluoromethylphenyl)-1,4-pentadien-3-one

https://huagongshe.com/ko/reaction/77658

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물WaterHCID 962—
반응물Sodium HydroxideHCID 14798—
반응물o-(Trifluoromethyl)benzaldehydeHCID 123067—
용매EthanolHCID 702—
생성물1,5-Bis(2-trifluoromethylphenyl)-1,4-pentadien-3-oneHCID 8543407988.7%

반응 단계

2-(Trifluoromethyl)-benzaldehyde (1w, 0.75 ml, 5.7 mmol) and acetone (19, 0.21 ml, 2.8 mmol) were combined in ethanol (20 ml) and stirred for 10 min at room temperature. A solution of sodium hydroxide (0.34 g, 8.5 mmol) and water (15 ml) was added and the mixture stirred for 18 hr at room temperature. The resulting precipitate was filtered and recrystallized from ethanol to afford 0.92 g (87%) of a yellow solid: mp 131-133° C. [expected mp 131° C.]; 1H NMR: δ 6.99 (d, 2H, J=15.9 Hz), 7.48 (t, 2H, J=7.6 Hz), 7.56 (t, 2H, J=7.0 Hz), 7.70 (d, 2H, J=7.7 Hz), 7.77 (d, 2H, J=7.6 Hz), 8.07 (d, 2H, J=15.7 Hz); 13C NMR: δ 123.9, 126.2, 127.9, 128.8, 129.4, 129.7, 132.1, 133.7, 139.1, 188.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841326B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-c9985af20dab4ee99bc1dd8b010eb9cc
출처 메모uspto-grants-2014_09