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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480443Generated: October 30, 2026

Water → 9,9-dihexylfluorene

https://huagongshe.com/reaction/480443

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 ml (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 numberUS06650047B2
Source datasetuspto-grants-2003_11
ORD IDord-2fbcf5d7e8d64941b0bf3da9948559e3
Source noteuspto-grants-2003_11