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HRID 3619生成日期:2026年10月23日

环戊二烯 → Dimethyl(2,7-di-tert-butylfluorenyl)cyclopentadienylsilane

https://huagongshe.com/zh-CN/reaction/3619

反应方程式

参与物

角色名称HCID投料
反应物环戊二烯HCID 7612—
反应物Dimethyl(2,7-di-tert-butylfluorenyl)chlorosilaneHCID 22495163—
反应物正丁基锂HCID 178418339—
溶剂聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
溶剂氧HCID 977—
溶剂正己烷HCID 8058—
产物Dimethyl(2,7-di-tert-butylfluorenyl)cyclopentadienylsilaneHCID 13172058952.3%

反应步骤

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.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US05733991
来源数据集uspto-grants-1998_03
ORD IDord-2b4ebe9966634e10a9ec36b7cb413dc4
来源说明uspto-grants-1998_03