化工社化工社 化学情報印刷レポート · 研究参考用
Ammonia → 1-(8-Quinolyl)-2,3-dimethylcyclopentadiene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 2-Cyclopenten-1-one, 2,3-dimethyl- | HCID 14270 | — |
| 反応物 | 8-Bromoquinoline | HCID 140109 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-(8-Quinolyl)-2,3-dimethylcyclopentadiene | HCID 22352124 | 41.4% |
反応手順
5 ml of n-BuLi (2.5 M in hexane, 12.5 mmol) were added dropwise at −95° C. to a solution of 2.5 g of 8-bromoquinoline (12 mmol) in 120 ml of THF, the mixture was stirred for 15 minutes, and 1.3 g of 2,3-dimethylcyclopent-2-enone (12 mmol) dissolved in 10 ml of THF were subsequently added. After warming to room temperature, the solution was refluxed for one hour. The cooled reaction mixture was hydrolyzed using ice, acidified using hydrochloric acid and then neutralized using ammonia solution. The aqueous phase was extracted with diethyl ether, and the combined organic phases were dried. Distillation at 150° C./0.05 mbar gave 1.1 g of 1-(8-quinolyl)-2,3-dimethylcyclopentadiene (40%) as a yellow, viscous oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06699948B2 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-f017544e06f04fcd845165beadfa3de0 |
| 出典メモ | uspto-grants-2004_03 |