Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → 1,1-Cyclopentadienyl(9-fluorenyl)dipenylmethane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Fluorene | HCID 6853 | — |
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | Diphenyl Fulvene | HCID 22238549 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 촉매 | HCID 178420589 | HCID 178420589 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1,1-Cyclopentadienyl(9-fluorenyl)dipenylmethane | HCID 22735132 | 42% |
반응 단계
Diphenylmethylene(9-fluorenyl)(cyclopentadienyl)zirconium dichloride ##STR11## 12.3 cm3 (30.7 mmol) of a 2.5 molar solution of n-butyllithium in hexane were slowly added to a solution of 5.10 g (30.7 mmol) of fluorene in 60 cm3 of tetrahydrofuran at room temperature. After 40 minutes, 7.07 g (30.7 mmol) of diphenylfulvene were added to the orange solution and the mixture was stirred overnight. 60 cm3 of water were added to the dark red solution, whereupon the solution became yellow in color, and the solution was extracted with ether. The ether phase was dried over MgSO4 and concentrated and the concentrate was left to crystallize at -35° C. 5.1 g (42%) of 1,1-cyclopentadienyl-(9-fluorenyl)diphenylmethane were obtained as a beige powder.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05232993 |
| 출처 데이터셋 | uspto-grants-1993_08 |
| ORD ID | ord-162d04fd3c194e18bd2a055ac47bf836 |
| 출처 메모 | uspto-grants-1993_08 |