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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48062생성일: 2026년 10월 24일

1-Diethoxyphosphorylpropan-2-one → 4-[3-(Trifluoromethoxy)phenyl]-3-buten-2-one

https://huagongshe.com/ko/reaction/48062

반응식

참여 물질

역할이름HCID투입량
반응물1-Diethoxyphosphorylpropan-2-oneHCID 14028—
반응물Sodium HydroxideHCID 14798—
반응물3-(Trifluoromethoxy)benzaldehydeHCID 605139—
촉매Tetrabutylammonium IodideHCID 67553—
용매DichloromethaneHCID 6344—
생성물4-[3-(Trifluoromethoxy)phenyl]-3-buten-2-oneHCID 6934411854%

반응 단계

Ex-626A) Tetrabutylammonium iodide (0.4 g, 0.05 mol) was added to a well-stirred biphasic mixture of 12 mL of 50% NaOH and 20 mL of methylene chloride under a nitrogen atmosphere. A solution of 3-trifluoromethoxybenzaldehyde (4.0 g, 0.021 mol) and diethyl (2-oxopropyl)phosphonate (4.08 g, 0.021 mol) in 4.0 mL of methylene chloride was added dropwise to the stirred solution. The resulting mixture was stirred at room temperature for 15 min, then quenched with water and extracted with hexane. The hexane layer was dried over MgSO4. The crude product was purified by flash column chromatography on silica gel eluting with 1:10 ethyl acetate in hexane to give 2.6 g (54%) of the desired 4-[3-(trifluoromethoxy)phenyl]-3-buten-2-one product as a yellow oil. 1H NMR (CDCl3) δ7.43 (m, 4H), 7.20 (d, 1H), 6.65 (d, 2H), 2.29 (s, 3H). 19F NMR (CDCl3) δ−62.05 (s, 3F).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699898B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-0ae043e1bfba43f78f3d7cfab4c39611
출처 메모uspto-grants-2004_03