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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913593Generated: October 26, 2026

Fluorene → 2-(3-Tert-butyl-5-methylcyclopentadienyl)-2-fluorenylpropane

https://huagongshe.com/reaction/1913593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFluoreneHCID 6853—
ReactantHexaneHCID 8058—
Reactant1,6,6-Trimethyl-3-tert-butyl-fulveneHCID 2762761—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(3-Tert-butyl-5-methylcyclopentadienyl)-2-fluorenylpropaneHCID 13172512018.2%

Reaction Steps

In a nitrogen atmosphere, a hexane solution of n-butyllithium (40 ml, 61.6 mmol) was added dropwise to a solution of fluorene (10.1 g, 60.8 mmol) in THF (300 ml) with ice cooling. The mixture was stirred at room temperature for 5 hours (resulting in a dark brown solution). The solution was ice cooled again, and a solution of 3-tert-butyl-1,6,6-trimethylfulvene (11.7 g, 66.5 mmol) in THF (300 ml) was added thereto dropwise in a nitrogen atmosphere. The reaction solution was stirred at room temperature for 14 hours. The resultant brown solution was ice cooled, and water (200 ml) was added. The obtained solution was extracted with diethyl ether. Then the organic phase was separated therefrom, and dried over magnesium sulfate. The organic phase was filtered, and the solvent was removed from the filtrate under reduced pressure, resulting in an orange-brown oil. The oil was purified by silica gel column chromatography (developing solvent: hexane) to give 3.8 g of a yellow oil. The analytical data are given below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609769B2
Source datasetuspto-grants-2013_12
ORD IDord-50903bc50da143429947ac75ec4aebfe
Source noteuspto-grants-2013_12