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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3619Generated: October 23, 2026

Cyclopentadiene → Dimethyl(2,7-di-tert-butylfluorenyl)cyclopentadienylsilane

https://huagongshe.com/en/reaction/3619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentadieneHCID 7612—
ReactantDimethyl(2,7-di-tert-butylfluorenyl)chlorosilaneHCID 22495163—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventOxygenHCID 977—
SolventHexaneHCID 8058—
ProductDimethyl(2,7-di-tert-butylfluorenyl)cyclopentadienylsilaneHCID 13172058952.3%

Reaction Steps

8.5 ml (21 mmol) of a 2.5M solution of butyllithium in hexane were added dropwise to 1.4 g (21 mmol) of cyclopentadiene in 45 ml of O2 -free and H2O-free THF at 0° C. under argon and the mixture was stirred for a further 2 hours at room temperature. This solution was subsequently added at room temperature to a solution of 7.9 g (21 mmol) of 2 in 100 ml of O2 -free and H2O-free THF over a period of 2 hours and the mixture was stirred for a further 1 hour at room temperature. 50 ml of H2O were added, the phases were separated and the aqueous phase was further extracted twice with 30 ml of Et2O each time. The combined organic phases were dried (MgSO4) and the solvent was removed in vacuo. After chromatography on 200 g of silica gel (hexane/methylene chloride 20:1), 4.4 g (51%) of 3 were obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05733991
Source datasetuspto-grants-1998_03
ORD IDord-2b4ebe9966634e10a9ec36b7cb413dc4
Source noteuspto-grants-1998_03