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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

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-(fluoren-9-yl)-hex-1-eneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616752
Source datasetuspto-grants-1997_04
ORD IDord-148dfe71f70c48ce8b460ab8bbcc455a
Source noteuspto-grants-1997_04