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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251530Generated: November 3, 2026

Hexane → 1-Cyclopentadienyl-1-(2,7-di-tert-butylfluorenyl)cyclohexane

https://huagongshe.com/reaction/1251530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant2,7-Di-tert-butylfluoreneHCID 4090082—
ReactantCyclohexylfulveneHCID 22327799—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-Cyclopentadienyl-1-(2,7-di-tert-butylfluorenyl)cyclohexaneHCID 13172310467.9%

Reaction Steps

To a THF (30 ml) solution including 5.0 g (18.6 mmol) of 2,7-di-tert-butylfluorene, a hexane solution (13.5 ml, 21.6 mmol) of n-butyllithium was added dropwise at −78° C. under nitrogen, followed by stirring at room temperature for 6 hours. Next, a THF (20 ml) solution including 3.42 g (23.4 mmol) of cyclohexylfulvene was added dropwise at 0° C. under a nitrogen atmosphere, followed by stirring at room temperature for 16 hours. The resultant reaction solution was decomposed with cold water, and then extracted with ether. The extract was dried over magnesium sulfate and then filtered, and the used solvent was removed from the filtrate under reduced pressure, thereby obtaining a solid. This solid was recrystallized from methanol to obtain 5.36 g of a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342568B1
Source datasetuspto-grants-2002_01
ORD IDord-7c02aa446e3949f4a0b6f1a920c296a1
Source noteuspto-grants-2002_01