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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1085628생성일: 2026년 10월 27일

Water → 1,5-Bis(3,4,5-trimethoxyphenyl)penta-1,4-dien-3-one

https://huagongshe.com/reaction/1085628

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Ethyl AcetateHCID 8857—
반응물3-(N,N,N-trimethylammonio)-1-(3,4,5-trimethoxyphenyl)propan-1-one iodideHCID 10409222—
생성물1,5-Bis(3,4,5-trimethoxyphenyl)penta-1,4-dien-3-oneHCID 383405—

반응 단계

3-(N,N,N-trimethylammonio)-1-(3,4,5-trimethoxyphenyl)propan-1-one iodide (355.9 g, 0.87 mole) was suspended in a mixture of water (3.56 L) and of ethyl acetate (2.54 L) and refluxed with rapid stirring for 2-3 hours. The mixture was cooled and the pale yellow organic layer was removed. Fresh ethyl acetate (2 L) was added and the mixture was refluxed for 1 hour, and the process was repeated once again. The organic layers were combined, washed with brine, dried over anhydrous MgSO4, and evaporated to dryness to provide a yellow oil, which was crystallized from hexane/ether to give 3,4,5-trimethoxyphenylvinyl ketone (m.p. 45°-47° C.). 200 MHz 1H NMR (CDCl3): δ 3.94 (9H, s, 3 OCH3), 5.92 (1H, dd, J=1.5 Hz, J=9 Hz), 6.44 (1H, dd, J=1.5 Hz, J=1.5 Hz, J=16 Hz), 7.18 (1H, dd, J=16 Hz, J=9 Hz), 7.28 (2H, H2 and H6).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05010100
출처 데이터셋uspto-grants-1991_04
ORD IDord-1d344d6e311a4bccb1db48ae8e8a97d1
출처 메모uspto-grants-1991_04