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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271013Generated: October 27, 2026

Hexane → 1-(Cyclopentadienyl)-1(3,6-di-tert-butylfluorenyl)diphenylmethane

https://huagongshe.com/reaction/271013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant6,6'-DiphenylfulveneHCID 101236—
Reactant3,6-DI-Tert-butylfluoreneHCID 11140437—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(Cyclopentadienyl)-1(3,6-di-tert-butylfluorenyl)diphenylmethaneHCID 131725132—

Reaction Steps

To a solution of 2.5 g (9.0 mmol) of 3,6-di-tert-butylfluorene in 40 ml of THF, 6.1 ml (9.8 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 4 hours. The resulting solution was ice cooled again, and thereto was dropwise added a solution of 2.5 g (10.8 mmol) of 6,6-diphenylfulvene in 30 ml of THF in a nitrogen atmosphere, followed by stirring at room temperature for 5 hours. Then, 50 ml of water was added. The organic phase extracted with diethyl ether and separated was dried over magnesium sulfate and then filtered. From the filtrate, the solvent was removed under reduced pressure to obtain a solid. The solid was recrystallized from methanol to obtain 3.4 g of a slightly yellow solid. The analyzed values are given below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449533B2
Source datasetuspto-grants-2008_11
ORD IDord-fdd4fd1d36724939ab4e70a4cd188de9
Source noteuspto-grants-2008_11