化工社化工社 化学情報印刷レポート · 研究参考用
Dimethylformamide → N,5-Dimethyl-3-phenyl-4-isoxazolecarboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Methylamine | HCID 6329 | — |
| 反応物 | 5-Methyl-3-phenylisoxazole-4-carboxylic acid | HCID 14343 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 溶媒 | 1,2-Dichloroethane | HCID 11 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | N,5-Dimethyl-3-phenyl-4-isoxazolecarboxamide | HCID 4104650 | — |
反応手順
To a suspension of 50.0 g (0.25 mol) of 5-methyl-3-phenyl-isoxazole-4-carboxylic acid in 1.2 l of 1,2-dichloroethane (DCE) is added 1.9 ml dimethyl formamide (DMF) and 21.4 ml (0.3 mol, 1.2 eq.) of thionyl chloride. The mixture is stirred for 2 h at reflux until a clear, yellow solution is formed. The solution is cooled to room temperature and then slowly added to a 8M solution of methylamine in ethanol (146 ml) at 5° C. The suspension is poured onto methylene chloride, washed with sat. NaHCO3-solution, dried over Na2SO4 and concentrated. This yields 52.3 g (99%) of the title compound as light brown solid, which is used for further reaction without purification. Mass spectrum: m/z (M+H)+: 217.1
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07087756B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-9f2d7503c50f422082db2b1fd2579b77 |
| 出典メモ | uspto-grants-2006_08 |