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Fluorene → 1,1-Cyclopentadienyl(9-fluorenyl)dipenylmethane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Fluorene | HCID 6853 | — |
| 反応物 | Hexane | HCID 8058 | — |
| 反応物 | Diphenyl Fulvene | HCID 22238549 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1,1-Cyclopentadienyl(9-fluorenyl)dipenylmethane | HCID 22735132 | 42% |
反応手順
Diphenylenemethylene(9-fluorenyl)(cyclopentadienyl)zirconium dichloride ##STR11## 12.3 cm3 (30.7 mmol) of a 2.5 molar hexane solution of n-butyllithium were slowly added to a solution of 5.10 g (30.7 mmol) of fluorene in 60 cm3 of THF 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, as a result of which the solution turns yellow, and the solution was extracted with ether. The ether phase was dried over MgSO4, concentrated, and allowed to crystallize at -35° C. 5.1 g (42%) of 1,1-cyclopentadienyl-(9-fluorenyl)diphenylmethane was obtained as a beige powder.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05663268 |
| 出典データセット | uspto-grants-1997_09 |
| ORD ID | ord-2ba957d05f104a3588cc47ed587a0aa0 |
| 出典メモ | uspto-grants-1997_09 |