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1-Diethylamino-6-(3,4-dimethoxyphenyl)hexan-3-one → 2-Ethylcyclopentane-1,3-dione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-Diethylamino-6-(3,4-dimethoxyphenyl)hexan-3-one | HCID 21485415 | — |
| 反応物 | 6-(3,4-Dimethoxyphenyl)hex-1-en-3-one | HCID 21485732 | — |
| 溶媒 | Potassium Hydroxide | HCID 14797 | — |
| 生成物 | 2-Ethylcyclopentane-1,3-dione | HCID 69978 | — |
反応手順
Reflux 6-(3,4-dimethoxyphenyl)hex-1-en-3-one, containing a small amount of 6-(3,4-dimethoxyphenyl)-1-diethylaminohexan-3-one (6 g, produced by slow distillation of the latter substance) with 2-ethylcyclopentane-1,3-dione (3.5 g) in 0.12% anhydrous methanolic potassium hydroxide (10 cc) for 10 hours. Remove most of the methanol under reduced pressure, add benzene (25 cc) and ether (25 cc) and wash the solution with water, dilute aqueous potassium hydroxide, dilute hydrochloric acid and water. Dry and evaporate the solvent to give the triketone adduct 2-[6-(3,4-dimethoxyphenyl)-3-oxohexyl]-2-ethylcyclopentane-1,3-dione; infrared absorption (gum) 5.80, 6.25 μ (split peak).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04002746 |
| 出典データセット | uspto-grants-1977_01 |
| ORD ID | ord-237a621020b4448eb6466d47d36f2cc4 |
| 出典メモ | uspto-grants-1977_01 |