関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methyl iodide | HCID 6328 | — |
| 反応物 | 3-Butenal, 2-methyl-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)- | HCID 93952 | — |
| 反応物 | Magnesium | HCID 5462224 | — |
| 反応物 | HCID 178418373 | HCID 178418373 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 3-Methyl-5-(2,6,6-trimethyl-2-cyclohexenyl)-4-penten-2-ol | HCID 53878389 | 77.8% |
反応手順
A solution of methylmagnesium iodide, prepared from 11 g of magnesium shavings and 76 g of methyl iodide, in 700 ml of absolute ether is added dropwise at -10° C. under nitrogen to a solution of 62 g of 2-methyl-4-(2,6,6-trimethyl-2-cyclohexenyl)-3-butenal in 700 ml of ether. The mixture is stirred for 4 hours at 30° C. and then poured on to an excess of ice-cold ammonium chloride solution. The mixture is extracted with ether in the usual manner, the extract is washed neutral with water and dried over anhydrous sodium sulphate to give, after removal of the solvent, 66 g of a yellow, slightly viscous oil which, after distillation in vacuo, yields 52 g of 3-methyl-5-(2,6,6-trimethyl-2-cyclohexenyl)-4-penten-2-ol; b.p.0.008 = 90°; nD20 = 1.4890. This alcohol has a very fine, tenacious sandalwood odour.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04046716 |
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| 出典データセット | uspto-grants-1977_09 |
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| ORD ID | ord-d74cf7cee1f44a459642b0b7cd91511f |
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| 出典メモ | uspto-grants-1977_09 |
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