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Ethyl 2-(triphenylphosphoranylidene)propionate → (E)-ethyl 2-methyl-3-(3,4,5-trifluorophenyl)acrylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl 2-(triphenylphosphoranylidene)propionate | HCID 79792 | — |
| 反応物 | 3,4,5-Trifluorobenzaldehyde | HCID 2776954 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (E)-ethyl 2-methyl-3-(3,4,5-trifluorophenyl)acrylate | HCID 12016766 | 93% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08541448B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-7ecd15a1db994d2ba591a4850e4ffa65 |
| 出典メモ | uspto-grants-2013_09 |