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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865407Generated: November 1, 2026

Fluorene → 5-Cyclopentadienyl-5-(9-fluorenyl)-1-hexene

https://huagongshe.com/reaction/865407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFluoreneHCID 6853—
Reactant6-Butenyl-6-methylfulveneHCID 54053322—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178506660HCID 178506660—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product5-Cyclopentadienyl-5-(9-fluorenyl)-1-hexeneHCID 15861916—

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-cyclopentadienyl-5-(9-fluorenyl)-1-hexene in a form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05565592
Source datasetuspto-grants-1996_10
ORD IDord-2749dd0b75e345b894264ea6464cdd11
Source noteuspto-grants-1996_10