HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ammonia → 1-(8-Quinolyl)-2,3-dimethylcyclopentadiene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ammonia | HCID 222 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 2-Cyclopenten-1-one, 2,3-dimethyl- | HCID 14270 | — |
| Edukt | 8-Bromoquinoline | HCID 140109 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(8-Quinolyl)-2,3-dimethylcyclopentadiene | HCID 22352124 | 41,4% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06437161B1 |
| Quelldatensatz | uspto-grants-2002_08 |
| ORD ID | ord-8020174ca987460abab882a768bda778 |
| Quellennotiz | uspto-grants-2002_08 |