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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613023Generated: November 1, 2026

Fluorene → HCID 18469391, compound

https://huagongshe.com/reaction/1613023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFluoreneHCID 6853—
Reactant1,1-DibromoethaneHCID 11201—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18469391HCID 18469391—

Reaction Steps

In this reaction, 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, this solution was added gradually to a stirred solution of 9 ml (0.1 m) of dibromoethane in 300 ml of pentane within 2 hours. Then the reaction mixture was treated with 50 ml of an aqueous NH4Cl solution, and then washed with 50 ml of water. The organic phase was dried over Na2SO4. Then the solvent was removed in vacuo. The yellow residue was dissolved in pentane. The pentane solution was filtered over silica. The solution was concentrated to about 20% of the original volume and then the product was crystallized at -30° C. A yield of 10.88 g of 1-bromo-2-(fluorenyl)ethane was obtained. The product was characterized through 1H NMR, 13C NMR, an Mass spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05191132
Source datasetuspto-grants-1993_03
ORD IDord-b5cb264228e440bd9509130bc115971e
Source noteuspto-grants-1993_03