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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271012Generated: October 30, 2026

Hexane → 2-(3-Tert-butyl-5-methylcyclopentadienyl)-2-(2,7-di-tert-butylfluorenyl)propane

https://huagongshe.com/reaction/271012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant2,7-Di-tert-butylfluoreneHCID 4090082—
Reactant2-tert-Butyl-5-(propan-2-ylidene)cyclopenta-1,3-dieneHCID 14688283—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(3-Tert-butyl-5-methylcyclopentadienyl)-2-(2,7-di-tert-butylfluorenyl)propaneHCID 13172513171.5%

Reaction Steps

To a solution of 2.45 g (8.80 mmol) of 2,7-di-tert-butylfluorene in 50 ml of THF, 5.67 ml (9.24 mmol) of a hexane solution of n-butyllithium was dropwise added in a nitrogen atmosphere at 0° C., followed by stirring at room temperature overnight. To the resulting solution, a solution of 2.85 g (17.6 mmol) of 3-tert-butyl-6,6-dimethylfulvene in 30 ml of THF was successively dropwise added in a nitrogen atmosphere at 0° C., followed by stirring at room temperature overnight to perform reaction. After the reaction, 30 ml of water was added. The organic phase was extracted with ether and dried over anhydrous magnesium sulfate. From the resulting solution, the solvent was distilled off to obtain a crude yellow solid. The solid was washed with methanol to obtain 2.77 g of a powdery white solid (yield: 71.5%.The analyzed values are given below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449533B2
Source datasetuspto-grants-2008_11
ORD IDord-b4278bf42cd34cd9b393c95076c5b4f5
Source noteuspto-grants-2008_11