化工社化工社 化学情報印刷レポート · 研究参考用
Isobutylamine → Ethyl 3-(2-isobutylcarbamoylphenyl)-2-methylacrylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Isobutylamine | HCID 6558 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | O-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733286 | — |
| 反応物 | 2-(2-Ethoxycarbonylpropen-1-yl)benzoic acid | HCID 69054538 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Ethyl 3-(2-isobutylcarbamoylphenyl)-2-methylacrylate | HCID 69060490 | 79.5% |
反応手順
Ethyl 3-(2-isobutylcarbamoylphenyl)-2-methylacrylate is prepared as described in Example 30, starting with 1.17 g (5.0 mmol) of 2-(2-ethoxycarbonylpropen-1-yl)benzoic acid in 10 cm3 of dimethylformamide, a solution of 0.69 cm3 (5.0 mmol) of triethylamine, 1.64 g (5.0 mmol) of O-[(cyano(ethoxycarbonyl)methylene)amino]-1,1,3,3-tetramethyluronium tetrafluoroborate (“TOTU”) in 6 cm3 of dimethylformamide and a second solution consisting of 366 mg (5.0 mmol) of isobutylamine, 0.69 cm3 (5.0 mmol) of triethylamine in 10 cm3 of dimethylformamide. 1.15 g of ethyl 3-(2isobutylcarbamoylphenyl)-2-methylacrylate are thus obtained in the form of a yellowish oil, which can be reacted in the following step without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07078428B2 |
| 出典データセット | uspto-grants-2006_07 |
| ORD ID | ord-4367c72295bc4b1ba1276fa164677eda |
| 出典メモ | uspto-grants-2006_07 |