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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
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 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 residue was left to crystallize at −35° C. 5.1 g (42%) of 1,1-cyclopentadienyl-(9-fluorenyl)diphenylmethane were obtained as a beige powder.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06713426B1 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-7088ca75658747c6aa2a2c7432e03144 |
| 出典メモ | uspto-grants-2004_03 |