化工社化工社 化学情報印刷レポート · 研究参考用
Sodium Iodide → 1-[4-(3-Piperidin-1-ylpropoxy)phenyl]ethanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Iodide | HCID 5238 | — |
| 反応物 | 4'-Hydroxyacetophenone | HCID 7469 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | N-(3-chloropropyl)piperidine hydrochloride | HCID 79624 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | Ammonia | HCID 222 | — |
| 生成物 | 1-[4-(3-Piperidin-1-ylpropoxy)phenyl]ethanone | HCID 2200112 | 6.8% |
反応手順
A mixture of 5.97 g of 4′-hydroxyacetophenone (43.8 mmol), 13.0 g of 1-(3-chloropropyl)-piperidine hydrochloride (65.8 mmol), 12.70 g of potassium carbonate (91.89 mmol), and 3.28 g of sodium iodide (21.9 mmol) in 100 mL dry acetone was stirred at reflux. After 1.5 h, the reaction was cooled to room temperature, filtered and concentrated. Ethyl acetate was added and the white solid that remained was filtered off. The filtrate was concentrated in vacuo and the crude residue was purified via silica gel chromatography using a gradient of ethyl acetate then 400:20:10 ethyl acetate: 7N ammonia in methanol:methanol to yield 583 mg of 1-[4-(3-piperidin-1-ylpropoxy)phenyl]ethanone as an oil. MS m/z 265 (M+H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08207168B2 |
| 出典データセット | uspto-grants-2012_06 |
| ORD ID | ord-b682f420bbec46bfa892f79c2171f154 |
| 出典メモ | uspto-grants-2012_06 |