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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252512Generated: November 3, 2026

Water → 9,9-dihexylfluorene

https://huagongshe.com/reaction/2252512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantFluoreneHCID 6853—
ReactantHexaneHCID 8058—
Reactant1-BromohexaneHCID 8101—
SolventTetrahydrofuranHCID 8028—
Product9,9-dihexylfluoreneHCID 512844995%

Reaction Steps

In the stream of dry nitrogen, 5.0 g (30 mmol) of fluorene was dissolved in dry tetrahydrofuran. To this solution, 22 m l (35 mmol) of a 1.6 M hexane solution of n-butylithium was added dropwise at −78° C., and the mixture was stirred at the temperature for 1 hour. To this was then added dropwise 4.9 ml (35 mmol) of n-hexyl bromide, and the mixture was stirred at −78° C. for 1 hour, and then at room temperature for 1 hour. To the resultant, 22 ml (35 mmol) of a 1.6 M hexane solution of n-butylithium was further added dropwise at −78° C., and the mixture was stirred at the temperature for 1 hour. To this was then added dropwise 4.9 ml (35 mmol) of n-hexyl bromide, and the mixture was stirred at −78° C. for 1 hour, and then at room temperature for 1 hour. Water was added dropwise to this mixture with ice-cooling, and the resultant was then subjected to extraction with ethyl acetate. The extract was dehydrated and dried over magnesium sulfate, and the solvent was then distilled off. The residue was subjected to recrystallization from hexane to obtain 9.5 g (95%) of 9,9-dihexylfluorene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323225B2
Source datasetuspto-grants-2008_01
ORD IDord-72f8b586cf574ea7bc65c7b4afb294c2
Source noteuspto-grants-2008_01