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HRID 1439839作成日:2026年10月25日

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

https://huagongshe.com/reaction/1439839

反応式

関与物質

役割名称HCID仕込み量
反応物(Bromo)(fluorenyl)methaneHCID 259258—
反応物HCID 178507085HCID 178507085—
溶媒Diethyl EtherHCID 3283—
生成物(Cyclopentadienyl)(fluorenyl)methaneHCID 13171779870%

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05496781
出典データセットuspto-grants-1996_03
ORD IDord-578ed21881c74915ba01378948d88b20
出典メモuspto-grants-1996_03