HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52678Generated: October 26, 2026
Fluorene → 5-(Cyclopentadienyl)-5-(fluoren-9-yl)-hex-1-ene
https://huagongshe.com/reaction/52678
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Fluorene | HCID 6853 | — |
| Reactant | 6-Butenyl-6-methylfulvene | HCID 54053322 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178506660 | HCID 178506660 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 5-(Cyclopentadienyl)-5-(fluoren-9-yl)-hex-1-ene | HCID 18622328 | — |
Reaction Steps
A solution was prepared by dissolving 10 g of fluorene in 100 mL of THF and then this was slowly reacted with 37.6 mL of a 1.6 molar solution of n-butyllithium in hexane. This dark red solution was stirred overnight at room temperature. Then a solution was prepared by combining 8.8 g of 6-(butenyl)-6-methylfulvene with 50 mL of THF. This solution was then added dropwise over a period of one half hour to the solution of the fluorenyl lithium salt. That reaction mixture was stirred overnight at room temperature and then 100 mL of water was added. The organic phase was dried overnight over sodium sulfate and the solvent was evaporated in a vacuum. The yellow residue was dissolved in pentane and filtered using silica gel. The solvent was concentrated by means of evaporation. Crystallization took place at about -18° C. to give 5-cyclopentdienyl-5-(9-fluorenyl)-1-hexene in a form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616752 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-148dfe71f70c48ce8b460ab8bbcc455a |
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| Source note | uspto-grants-1997_04 |
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