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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2688Erstellt: 24. Oktober 2026

Fluorene → 1,1-Cyclopentadienyl(9-fluorenyl)dipenylmethane

https://huagongshe.com/de/reaction/2688

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFluoreneHCID 6853—
EduktHexaneHCID 8058—
EduktDiphenyl FulveneHCID 22238549—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1,1-Cyclopentadienyl(9-fluorenyl)dipenylmethaneHCID 2273513242%

Reaktionsschritte

12.3 cm3 (30.7 mmol) of a 2.5 molar hexane solution of n-butyllithium were slowly added to a solution of 5.10 g (30.7 mmol) of fluorene in 60 cm3 of tetrahydrofuran at room temperature. 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, whereupon the solution became yellow in color, and the solution was extracted with ether. The ether phase was dried over MgSO4 and concentrated and the residue was left to crystallize at -35° C. 5.1 g (42%) of 1,1-cyclopentadienyl-(9-fluorenyl)diphenylmethane were obtained as a beige powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05731254
Quelldatensatzuspto-grants-1998_03
ORD IDord-1d2b61ecfe914348bdf9551b97784846
Quellennotizuspto-grants-1998_03