Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ammonia → 1-(8-Quinolyl)-2,3-dimethylcyclopentadiene
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ammonia | HCID 222 | — |
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 2-Cyclopenten-1-one, 2,3-dimethyl- | HCID 14270 | — |
| 반응물 | 8-Bromoquinoline | HCID 140109 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(8-Quinolyl)-2,3-dimethylcyclopentadiene | HCID 22352124 | 41.4% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06699948B2 |
| 출처 데이터셋 | uspto-grants-2004_03 |
| ORD ID | ord-f017544e06f04fcd845165beadfa3de0 |
| 출처 메모 | uspto-grants-2004_03 |