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HRID 50552作成日:2026年10月26日

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

https://huagongshe.com/reaction/50552

反応式

関与物質

役割名称HCID仕込み量
反応物FluoreneHCID 6853—
反応物HexaneHCID 8058—
反応物Diphenyl FulveneHCID 22238549—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物1,1-Cyclopentadienyl(9-fluorenyl)dipenylmethaneHCID 2273513242%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713426B1
出典データセットuspto-grants-2004_03
ORD IDord-7088ca75658747c6aa2a2c7432e03144
出典メモuspto-grants-2004_03