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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1439839생성일: 2026년 10월 24일

(Bromo)(fluorenyl)methane → (Cyclopentadienyl)(fluorenyl)methane

https://huagongshe.com/ko/reaction/1439839

반응식

참여 물질

역할이름HCID투입량
반응물(Bromo)(fluorenyl)methaneHCID 259258—
반응물HCID 178507085HCID 178507085—
용매Diethyl EtherHCID 3283—
생성물(Cyclopentadienyl)(fluorenyl)methaneHCID 13171779870%

반응 단계

The ligand (cyclopentadienyl)(fluorenyl)methane was prepared as follows. To 0.4 mole dibromomethane dissolved in 200 mL pentane was added 0.2 mole fluorenyllithium powder. After the addition was complete, the reaction mixture was stirred for two hours. The reaction mixture was filtered and the filtrate washed with 100 mL of distilled water. The organic phase was dried with Na2SO4 and the solvent was stripped under vacuum. The residue was washed with 150 mL pentane to remove unreacted fluorene and dried under vacuum to yield pale yellow colored (bromo)(fluorenyl)methane. The yield was 80%. The (bromo)(fluorenyl)methane was dissolved in 20 mL ether and 19 mL (2M in THF) cyclopentadienylsodium was added at a rate of 0.15 mL/min. The reaction mixture was stirred for two hours and washed with 50 mL distilled water. The organic phase was dried over Na2SO4 and the solvent removed under vacuum to yield pale yellow (cyclopentadienyl)(fluorenyl)methane. The yield was 70%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05496781
출처 데이터셋uspto-grants-1996_03
ORD IDord-578ed21881c74915ba01378948d88b20
출처 메모uspto-grants-1996_03