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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080833Generated: October 26, 2026

Dibromomethane → (Bromo)(fluorenyl)methane

https://huagongshe.com/reaction/1080833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromomethaneHCID 3024—
ReactantHCID 178506660HCID 178506660—
SolventPentaneHCID 8003—
Product(Bromo)(fluorenyl)methaneHCID 259258—
Product(Cyclopentadienyl)(fluorenyl)methaneHCID 131717798—

Reaction Steps

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 (2 M 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%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05583189
Source datasetuspto-grants-1996_12
ORD IDord-6543958718984be8a852a0bc4eac3dae
Source noteuspto-grants-1996_12