化工社化工社 化学情報印刷レポート · 研究参考用
Imidazole → Trimethyl[(2-methyl-1-phenoxybut-3-yn-2-yl)oxy]silane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Imidazole | HCID 795 | — |
| 反応物 | Chlorotrimethylsilane | HCID 6397 | — |
| 反応物 | Diethylether water | HCID 21584184 | — |
| 反応物 | 2-Methyl-1-phenoxybut-3-yn-2-ol | HCID 23266458 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Trimethyl[(2-methyl-1-phenoxybut-3-yn-2-yl)oxy]silane | HCID 21325376 | — |
反応手順
The hydroxyl group of this alkyne is protected by dissolving 2 parts of the butyne in 5 parts by volume of dimethylformamide and successively treating the reaction mixture with 2 parts of imidazole and 1.2 parts of trimethylsilylchloride. The reaction mixture is stirred at room temperature for 1 hour and poured into ether/water. The ethereal layer is washed with water and dried over anhydrous sodium sulfate. Isolation by low pressure liquid chromatography on silica gel provides 3-methyl-3-trimethylsilyloxy-4-phenoxy-1-butyne.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04149006 |
| 出典データセット | uspto-grants-1979_04 |
| ORD ID | ord-2d05f06d6e454e9bb29f86245611036f |
| 出典メモ | uspto-grants-1979_04 |