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HRID 48062作成日:2026年10月26日

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

https://huagongshe.com/reaction/48062

反応式

関与物質

役割名称HCID仕込み量
反応物1-Diethoxyphosphorylpropan-2-oneHCID 14028—
反応物Sodium HydroxideHCID 14798—
反応物3-(Trifluoromethoxy)benzaldehydeHCID 605139—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒DichloromethaneHCID 6344—
生成物4-[3-(Trifluoromethoxy)phenyl]-3-buten-2-oneHCID 6934411854%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699898B2
出典データセットuspto-grants-2004_03
ORD IDord-0ae043e1bfba43f78f3d7cfab4c39611
出典メモuspto-grants-2004_03