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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075375Generated: October 25, 2026

Fluorene → 9-Hexyl-9-(5-cyano-5-methlhexyl)-fluorene

https://huagongshe.com/reaction/1075375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFluoreneHCID 6853—
Reactant1-BromohexaneHCID 8101—
Reactant6-Bromo-2,2-dimethylhexanenitrileHCID 4638215—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product9-Hexyl-9-(5-cyano-5-methlhexyl)-fluoreneHCID 69977936—

Reaction Conditions

Temperature-7.5 °C

Reaction Steps

2.4 g of butyllithium dissolved in 15 ml of hexane was slowly added during 5 minutes into 6.0 g of fluorene dissolved in 40 ml of anhydrous tetrahydrofuran at -50° C. under nitrogen protection. The mixture was stirred at -30 to 15° C. for 1 hour before it was cooled again to -40 ~-50° C. Then, 6.0 g of 1-bromohexane was added in 5 minutes. The mixture was subsequently stirred for 2 hours while the temperature was gradually increased to room temperature. The mixture was then cooled to -50° C., and 2.4 g of butyllithium dissolved in 15 ml of hexane was slowly added in 5 minutes under nitrogen protection. The mixture was stirred at -30 to 15° C. for 1 hour before it was cooled again to -40~-50° C. Then, 7.6 g of 6-bromo-2,2-dimethylhexanenitrile was added in 5 minutes. The mixture was subsequently stirred for 15 hours at room temperature, dispersed in water, and extracted with ether. The etheral solution was washed with water and brine, dried with magnesium sulfate, and evaporated. The residue was distilled to collect 12.4 g (92%) of light yellow liquid. MS (m/z): 373 (M+), 288, 249, 217, 191, 179, 165.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05900327
Source datasetuspto-grants-1999_05
ORD IDord-ae0238323acb46f9af43d3973be69560
Source noteuspto-grants-1999_05