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Damascenone → 2,6,6-Trimethyl-1-(but-2-enoyl)-cyclohexa-1,3-dien-5-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Damascenone | HCID 62775 | — |
| 反応物 | Oxyselenide | HCID 167175 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 2,6,6-Trimethyl-1-(but-2-enoyl)-cyclohexa-1,3-dien-5-one | HCID 53817388 | 90.4% |
反応手順
2.5 g (13 mMole) of 2,6,6-trimethyl-1-(but-2-enoyl)-cyclohexa-1,3-dien [prepared according to the method given in Helv. Chim. Acta 54, 1899 (1971)] dissolved in 50 ml of dioxane were heated, under nitrogen atmosphere, during 45 min. at 60°, in the presence of 1.8 g (16 mMole) of selenium oxide. The reaction mixture was then cooled, concentrated under reduced pressure, and the obtained residue, diluted with 50 ml of acetic acid, was finally stirred at room temperature for 2 hours in the presence of 6 g of Raney nickel. The reaction mixture was then filtered, evaporated to dryness and the obtained residue was distilled (b.p. 100°-110°/o.2 Torr) to afford 2.4 g of a material containing 80 % of the desired keto compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US03957877 |
| 出典データセット | uspto-grants-1976_05 |
| ORD ID | ord-0ff78fe7c109440195d6ffb28d8d05d7 |
| 出典メモ | uspto-grants-1976_05 |