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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766639Generated: October 29, 2026

Fluorene → HCID 601495, compound

https://huagongshe.com/reaction/1766639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFluoreneHCID 6853—
Reactant1,1-DibromoethaneHCID 11201—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 601495HCID 60149570%

Reaction Steps

About 8.3 g (0.05 m) of fluorene was dissolved in 150 ml of tetrahydrofuran. Then 31.8 ml (0.05 m) of butyl lithium (1.6 molar in hexane) was added dropwise to this solution. After one hour, 2.3 ml (0.25 m) of dibromoethane in 25 ml of tetrahydrofuran was added. The solution was stirred for 3 hours. The yellow solution was washed with 50 ml of an aqueous NH4Cl solution (5 g NH4Cl/50 ml H2O), then washed with 50 ml of water and then the organic phase was dried over Na2SO4. Then the solvent was removed in vacuo. The light yellow residue was washed twice with 25 ml of pentane. The resulting product was white. The yield was 12.5 g, i.e. a yield of about 70%, based on the moles of fluorene reacted. The product was confirmed through 1H NMR, 13C NMR, mass spectroscopy, and gas chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230128B2
Source datasetuspto-grants-2007_06
ORD IDord-b248754f33d4461ab2b612718d806ec4
Source noteuspto-grants-2007_06