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Dimethylformamide → N-Butyl-N-(heptan-2-YL)aniline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Butyl bromide | HCID 8002 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | N-(2-Heptyl)aniline | HCID 11344519 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-Butyl-N-(heptan-2-YL)aniline | HCID 18000381 | 44% |
反応手順
A mixture of N-(1-methylhexyl)aniline (76 parts) 1-bromobutane (66 parts), anhydrous potasium carbonate (65 parts) and DMF (150 parts) was stirred while heating under reflux for 41 hours. An additional quantity of 1-bromo butane (44 parts) was added and the mixture stirred while heating under reflux for a further 19 hours. The cooled mixture was poured into water (400 parts) and the organic phase separated. The aqueous phase was extracted with toluene, the organic phases and toluene extract were combined and washed with water (2×100 arts) before evaporating to leave N-butyl-N-(1-methylhexyl)aniline (72.8 parts, 44%) which was purified by vacuum distillation to give N-butyl-N-(1-methylhexyl)aniline b.pt 73-80° C., 2.6 mm Hg.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06589296B1 |
| 出典データセット | uspto-grants-2003_07 |
| ORD ID | ord-3ff9c2ee28d742bc8f195bc18c3d982e |
| 出典メモ | uspto-grants-2003_07 |