HuagongsheHuagongshe Chemistry Print Report · For research reference only
Fluorene → 1,1-Cyclopentadienyl(9-fluorenyl)dipenylmethane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Fluorene | HCID 6853 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Diphenyl Fulvene | HCID 22238549 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,1-Cyclopentadienyl(9-fluorenyl)dipenylmethane | HCID 22735132 | 42% |
Reaction Steps
12.3 cm3 (30.7 mmol) of a 2.5 molar hexane solution of n-butyllithium were added slowly at room temperature to a solution of 5.10 g (30.7 mmol) of fluorene in 60 cm3 of THF. 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, the solution becoming a yellow color, and the solution was extracted with ether. The ether phase was dried over MgSO4, evaporated and left to crystallize at -35° C. 5.1 g (42%) of 1,1-cyclopentadienyl(9-fluorenyl)dipenylmethane were obtained as a beige powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05587501 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-0575f94ca7944391ae03911a9e71a1e2 |
| Source note | uspto-grants-1996_12 |