戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 45688作成日:2026年10月24日

Ethyl 2-(triphenylphosphoranylidene)propionate → (E)-ethyl 2-methyl-3-(3,4,5-trifluorophenyl)acrylate

https://huagongshe.com/ja/reaction/45688

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 2-(triphenylphosphoranylidene)propionateHCID 79792—
反応物3,4,5-TrifluorobenzaldehydeHCID 2776954—
溶媒DimethylformamideHCID 6228—
生成物(E)-ethyl 2-methyl-3-(3,4,5-trifluorophenyl)acrylateHCID 1201676693%

反応手順

To a solution of dry DMF (50 mL) under N2 was added 3,4,5-trifluorobenzaldehyde (4.26 g, 26.6 mmol) followed by ethyl 2-(triphenylphosphoranylidene)propionate (10.6 g, 29.3 mmol) in portions, keeping the solution at room temperature. After 1 hour, TLC (10% EtOAC in Hexanes) showed complete conversion, and the solvent was removed by rotary evaporation. The resulting material was brought up in 50 mL methyl t-butyl ether (MBTE) and the precipitate removed by filtration and washed with additional MBTE (3×50 mL). After concentration, the resulting filtrate was applied onto a silica gel column (25% EtOAc in hexanes) resulting in 6.0 g of the title compound (93%) as a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541448B2
出典データセットuspto-grants-2013_09
ORD IDord-7ecd15a1db994d2ba591a4850e4ffa65
出典メモuspto-grants-2013_09