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Imidazole → 4-Methyl-4-trimethylsilyloxy-7-oxa-1octyne
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 | Chlorotrimethylsilane | HCID 6397 | — |
| 反応物 | 4-Hydroxy-4-methyl-7-oxa-1-octyne | HCID 12786229 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | 4-Methyl-4-trimethylsilyloxy-7-oxa-1octyne | HCID 12786230 | — |
反応手順
To a solution of 13 g. (0.091 moles) of 4-hydroxy-4-methyl-7-oxa-1-octyne and 16 g. (0.235 moles) of imidazole in 80 ml. of dry dimethylformamide is added dropwise, at 5° C. under nitrogen with stirring, 12.5 ml. (0.115 moles) of trimethylchlorosilane. After an additional 15 minutes at 5° C. the solution is stirred at ambient temperature for 18 hours then added to 450 ml. of hexane. The resulting solution is washed with ice-cold water, ice-cold saturated sodium chloride solution, dried with anhydrous magnesium sulfate and taken to dryness in vacuo. Distillation of the residual oil furnishes 16.8 g. (86%) of product; b.p. 87°-88° C. (7 mm.).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04297516 |
| 出典データセット | uspto-grants-1981_10 |
| ORD ID | ord-775a5ff1cc3247dfb50c81e84f990401 |
| 出典メモ | uspto-grants-1981_10 |