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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495747Generated: October 27, 2026

Hexane → 2-(Cyclopentadienyl)-2-(3,6-di-tert-butylfluorenyl)propane

https://huagongshe.com/reaction/495747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant1,3-Cyclopentadiene, 5-(1-methylethylidene)-HCID 137467—
Reactant3,6-DI-Tert-butylfluoreneHCID 11140437—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(Cyclopentadienyl)-2-(3,6-di-tert-butylfluorenyl)propaneHCID 131725129—

Reaction Steps

To a solution of 3.0 g(10.8 mmol) of 3,6-di-tert-butylfluorene in 40 ml of THF, 7.0 ml (11.3 mmol) of a hexane solution of n-butyllithium was dropwise added in a nitrogen atmosphere with ice cooling, followed by stirring at room temperature for 6 hours. From the reaction mixture, the solvent was removed under reduced pressure, and the residue was washed with pentane and dried to obtain a white solid. To a solution of the solid in 30 ml of THF, a solution of 1.4 g (13.2 mmol) of 6,6-dimethylfulvene in 30 ml of THF was dropwise added in a nitrogen atmosphere with ice cooling, followed by stirring for 5 hours. Then, 30 ml of water was added. The organic phase extracted with diethyl ether and separated was dried over magnesium sulfate and filtered. From the filtrate, the solvent was removed under reduced pressure to obtain a solid. The solid was recrystallized from methanol to obtain 2.9 g of a slightly yellow solid. The analyzed values are given below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939928B1
Source datasetuspto-grants-2005_09
ORD IDord-976b8f1f1d654706831fb864bb6c1355
Source noteuspto-grants-2005_09