関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hexane | HCID 8058 | — |
| 反応物 | 1-(Trimethylsilyl)prop-1-yne | HCID 80363 | — |
| 反応物 | 1-(3-Bromoprop-1-yn-1-yl)-4-fluorobenzene | HCID 10560524 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (6-(4-Fluorophenyl)hexa-1,5-diynyl)trimethylsilane | HCID 66597810 | 99% |
反応手順
To a solution of trimethyl(prop-1-ynyl)silane (2.19 g, 19.50 mmol) in 22 mL of THF at −78° C., was added dropwise n-BuLi 2.5M in hexane (7.8 mL, 20 mmol). After stirring 2 hours at −78° C., 1-(3-bromoprop-1-ynyl)-4-fluorobenzene (1.40 g, 6.5 mmol) in 6 mL of THF was slowly added and the resulting mixture was stirred for 1 h at −78° C. and warmed to room temperature for an additional 1 h. The reaction mixture was quenched with water and extracted with ethyl acetate. The organic layer was dried over MgSO4, filtered and concentrated to afford 1.57 g of (6-(4-fluorophenyl)hexa-1,5-diynyl)trimethylsilane (99%) as a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08883826B2 |
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| 出典データセット | uspto-grants-2014_11 |
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| ORD ID | ord-6f4a3cd4ef624ad5944a351375f5c8fd |
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| 出典メモ | uspto-grants-2014_11 |
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