化工社化工社 化学情報印刷レポート · 研究参考用
Isopropanol → 2-Cyclohexen-1-one, 2,5,6-trimethyl-
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Isopropanol | HCID 3776 | — |
| 反応物 | Ethyl ketone | HCID 7288 | — |
| 反応物 | 3-Hydroxybutanal | HCID 7897 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 2-Cyclohexen-1-one, 2,5,6-trimethyl- | HCID 89264 | 47.1% |
反応手順
A mixture of 88 g of β-hydroxybutyraldehyde and 150 g of diethyl ketone is added dropwise in the course of one hour to a mixture of 250 g of diethyl ketone, 80 g of isopropanol and 5 g of sodium hydroxide powder which is boiling under reflux. The whole is boiled for another hour under reflux. Neutralization is effected with glacial acetic acid and the aqueous phase is separated. The organic layer is fractionated. 65 g of 2,5,6-trimethyl-2-cyclohexen-1-one having a boiling point of 74° to 76° C. at 12 mm Hg is obtained. The yield is 47% with reference to β-hydroxybutyraldehyde.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04128728 |
| 出典データセット | uspto-grants-1978_12 |
| ORD ID | ord-c16defd56be34a8fba979fa521f18f93 |
| 出典メモ | uspto-grants-1978_12 |