関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Glycerol | HCID 753 | — |
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | 4-Aminopyridine | HCID 1727 | — |
| 反応物 | Nitrobenzene | HCID 7416 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1,6-Naphthyridine | HCID 67488 | 18% |
反応手順
Glycerol (138.15 g, 1.5 mol) was added dropwise to an ice-cold mixture of "sulfo-mix" (a mixture of nitrobenzene and fuming sulfuric acid, see: Utermohlen, W. P., J. Org. Chem, 1943 8, 544). Addition of 4-aminopyridine (56.46 g, 0.6 mol) was followed by a rapid dropwise addition of water (225 ml), which caused a rise in temperature to 80°; the reaction mixture was allowed to stir until it became homogeneous, and was subsequently heated to 135° for 48 hours. It was then allowed to cool, poured into 1 l ice water, and the pH was adjusted to 13 by the addition of sodium hydroxide pellets. The resulting thick precipitate was removed by filtration, and the filtrate was extracted with methylene chloride (2×2 l). The combined organic extracts were dried over sodium sulfate, filtered, and concentrated to yield a crude product, which was purified by column chromatography (98:2 methylene chloride:methanol). The title product was obtained as an amber oil which crystallized upon standing (13.7 g, 0.11 mol, 18% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05214051 |
|---|
| 出典データセット | uspto-grants-1993_05 |
|---|
| ORD ID | ord-47fec2031798471085704012fec77a39 |
|---|
| 出典メモ | uspto-grants-1993_05 |
|---|