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)chlorosilane | HCID 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)cyclopentadienylsilane | HCID 131720589 | 52.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US05733991 |
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| 来源数据集 | uspto-grants-1998_03 |
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| ORD ID | ord-2b4ebe9966634e10a9ec36b7cb413dc4 |
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| 来源说明 | uspto-grants-1998_03 |
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