Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630584Generated: October 26, 2026

Hexane → Methyl(p-tolyl)cyclopentadienyl(2,7-diphenyl-3,6-di-tert-butylfluorenyl)methane

https://huagongshe.com/reaction/630584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant6-Methyl-6-(p-tolyl)fulveneHCID 21676448—
ReactantBenzyl(p-chlorophenyl)methylene(cyclopentadienyl)(2,7-diphenyl-3,6-di-tert-butylfluorene)HCID 131735408—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductMethyl(p-tolyl)cyclopentadienyl(2,7-diphenyl-3,6-di-tert-butylfluorenyl)methaneHCID 131735409—

Reaction Steps

Under a nitrogen atmosphere, a solution of n-butyllithium in hexane (6.3 ml, 10.2 mmol) was dropped into a solution of 2,7-diphenyl-3,6-di-tert-butylfluorene (4.0 g, 9.3 mmol) in dry tetrahydrofuran (50 ml) at −10° C., and then the product was stirred at room temperature for 20 hours. Then, 6-methyl-6-(p-tolyl)fulvene (1.9 g, 10.2 mmol) was dropped into this solution at −10° C., and the product was stirred at room temperature for 2 hours to induce a reaction. After the reaction was terminated, dilute aqueous hydrochloric acid was added thereto, the product was subjected to extraction with hexane, the organic layer was subsequently washed with water and then dehydrated with anhydrous magnesium sulfate, and then the solvent was distilled off to produce a light brown solid. The produced solid was recrystallized with methanol to obtain 5.1 g of an objective. The analytical values were as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315602B2
Source datasetuspto-grants-2016_04
ORD IDord-9ea0d5fa28814f3a8979288c0746ad30
Source noteuspto-grants-2016_04