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HRID 3619作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物CyclopentadieneHCID 7612—
反応物Dimethyl(2,7-di-tert-butylfluorenyl)chlorosilaneHCID 22495163—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒OxygenHCID 977—
溶媒HexaneHCID 8058—
生成物Dimethyl(2,7-di-tert-butylfluorenyl)cyclopentadienylsilaneHCID 13172058952.3%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05733991
出典データセットuspto-grants-1998_03
ORD IDord-2b4ebe9966634e10a9ec36b7cb413dc4
出典メモuspto-grants-1998_03