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9-(2-bromoethyl)-9H-fluorene → 9-(2-Vinylfluorenyl)-2-(9-Fluorenyl)ethane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 9-(2-bromoethyl)-9H-fluorene | HCID 11000215 | — |
| 反応物 | 2-ethenyl-9H-fluorene | HCID 11041607 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 9-(2-Vinylfluorenyl)-2-(9-Fluorenyl)ethane | HCID 86752827 | — |
反応手順
To 1.15 g (6.0 mmol) 2-vinylfluorene in 100 mL diethyl ether was added 3.75 mL (6.0 mmol) n-butyllithium (1.6M in hexane). The reaction mixture was stirred for 4 hours at room temperature. Then 1.64 g (6.0 mmol) 1-bromo-2-(9-fluorenyl)ethane was added and the mixture was stirred for 14 hours at room temperature. The precipitate was removed by filtration, washed with methanol, filtered with pentane using silica gel 60, and concentrated by evaporation under vacuum. The yield was 1.69 g (73%) 1-(9-(2-vinyl)fluorenyl)-2-(9-fluorenyl)ethane as a colorless solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05770755 |
| 出典データセット | uspto-grants-1998_06 |
| ORD ID | ord-cbdacd8506564f279f97bb5941f9fa7c |
| 出典メモ | uspto-grants-1998_06 |