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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50552생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/50552

반응식

참여 물질

역할이름HCID투입량
반응물FluoreneHCID 6853—
반응물HexaneHCID 8058—
반응물Diphenyl FulveneHCID 22238549—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1,1-Cyclopentadienyl(9-fluorenyl)dipenylmethaneHCID 2273513242%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713426B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-7088ca75658747c6aa2a2c7432e03144
출처 메모uspto-grants-2004_03