化工社化工社 化学情報印刷レポート · 研究参考用
Ethyl ketone → 2-Cyclohexen-1-one, 2,5,6-trimethyl-
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl ketone | HCID 7288 | — |
| 反応物 | 3-Methoxybutyraldehyde | HCID 98040 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 2-Cyclohexen-1-one, 2,5,6-trimethyl- | HCID 89264 | 56% |
反応手順
102 g of β-methoxybutyraldehyde is dripped in the course of one hour into a mixture of 500 g of diethyl ketone and 10 g of a 30% solution of sodium methylate in methanol which is boiling under reflux. The whole is then heated for another hour under reflux. The reaction mixture is processed as described in Example 2. 77 g of 2,5,6-trimethyl-2-cyclohexen-1-one is obtained, i.e. a 56% yield with reference to β-methoxybutyraldehyde.
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-9c14c87cead5429790577056f90c7ce5 |
| 出典メモ | uspto-grants-1978_12 |