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Imidazole → 3-Triethylsilyloxy-1-octyne
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Imidazole | HCID 795 | — |
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | 1-Octyn-3-ol | HCID 13166 | — |
| 反応物 | Chlorotriethylsilane | HCID 13819 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 溶媒 | Water hexane | HCID 22114717 | — |
| 生成物 | 3-Triethylsilyloxy-1-octyne | HCID 12675346 | — |
反応手順
To a magnetically stirred solution of 50 g of 1-octyn-3-ol, 83 g of imidazole, and 500 ml of anhydrous dimethylformamide, cooled in an ice-water bath under an argon atmosphere, is slowly added 90 g of chlorotriethylsilane. After several minutes the reaction mixture is warmed to ambient temperature, and the progress of the reaction is monitored by tlc (1:4/ethyl acetate:benzene). On completion, the reaction mixture is poured into 500 ml of an iced mixture of 1:1 hexane-water. The organic phase is separated, washed with water and brine, dried over sodium sulfate and concentrated in vacuo. The resulting oil is distilled to provide 83 g (bp 70°-72° C., 0.35 mm).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04233231 |
| 出典データセット | uspto-grants-1980_11 |
| ORD ID | ord-9524ce4d84364356a2c5d4e376b163b2 |
| 出典メモ | uspto-grants-1980_11 |