関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | 4-(Trifluoromethyl)aniline | HCID 9964 | — |
| 反応物 | Methyl 3-oxovalerate | HCID 121699 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Methyl 3-(4-trifluoromethylphenylamino)-2-pentenoate | HCID 68545758 | 72.8% |
反応手順
In a 1 L-flask were placed 4-trifluoromethylaniline (161 g, 1.00 mol), methyl 3-oxopentanoate (130 g, 1.00 mol) and toluene (160 mL). To this solution was added acetic acid (16 g, 0.27 mol), and the resulting mixture was heated in a bath kept at 100° C. under a reduced pressure of 19 kPa for 3.5 hours, while the water generated was taken out of the reaction system by using a Dean-Stark trap under reflux. Acetic acid (16 g, 0.27 mol) was then added, and reflux was continued for 4.5 hours. Acetic acid (8 g, 0.13 mol) was then added again, and reflux was continued for another 2.5 hours. The heating was then discontinued, nitrogen leaked in, and the reaction mixture cooled. After distillation of the solvent and acetic acid under reduced pressure, the residue was distilled under reduced pressure to give 199 g of the title compound. The yield was 72.8%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07601842B2 |
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| 出典データセット | uspto-grants-2009_10 |
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| ORD ID | ord-a5b7a54b457948e4a9b314aabba51ac7 |
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| 出典メモ | uspto-grants-2009_10 |
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