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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708652Generated: October 29, 2026

Fluorene → HCID 178506660, compound

https://huagongshe.com/reaction/1708652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFluoreneHCID 6853—
ReactantHCID 178418348HCID 178418348—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178506660HCID 178506660—

Reaction Steps

In a 300-cm3 four-necked flask in which the atmosphere was replaced with nitrogen, 7.4 g of fluorene were dissolved in 100 cm3 of tetrahydrofuran, followed by treating the solution with methyllithium, thereby obtaining a tetrahydrofuran solution of fluorenyllithium. Next, 50 cm3 of a tetrahydrofuran solution containing 5.2 g of previously synthesized 3,7-biscyclopentadienylidenebicyclo[3,3,0]octane were added dropwise to the tetrahydrofuran solution at -10° C. over 30 minutes. After completion of the addition, the reaction temperature was elevated up to room temperature, followed by stirring for 15 hours. Then, 100 cm3 of a 3.6% hydrochloric acid solution were poured thereinto to bring the reaction to an end. The resultant solid was collected by filtration, washed with ether, and then dried to obtain 7.6 g of white powdery 3,7-dicyclopentadienyl-3,7-difluorenylbicyclo[3,3,0]octane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05359102
Source datasetuspto-grants-1994_10
ORD IDord-7681e72b6c7d4950b55b4ab5e84aec7f
Source noteuspto-grants-1994_10