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Phosphorus oxychloride → 2-Chloro-6-methoxyquinoxaline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Phosphorus oxychloride | HCID 24813 | — |
| 反応物 | 7-Methoxy-1,2-dihydroquinoxalin-2-one | HCID 491319 | — |
| 反応物 | 6-Methoxyquinoxalin-2(1H)-one | HCID 13437707 | — |
| 生成物 | 2-Chloro-6-methoxyquinoxaline | HCID 12686412 | 35% |
反応手順
A mixture of 6-methoxyquinoxalin-2(1H)-one and 7-methoxyquinoxalin-2(1H)-one (5.67 g, 32.20 mmol) was refluxed in phosphorus oxychloride (120 mL) for 1 h. The reaction was concentrated and quenched by addition of ice, then basified with sodium carbonate, and extracted with ethyl acetate (3×200 mL). The organic layers were combined and concentrated in vacuo. The crude product was absorbed onto sodium sulfate and purified by column chromatography (0 to 5% ethyl acetate/hexanes) to afford 2-chloro-6-methoxyquinoxaline (2.21 g, 11.36 mmol, 35% yield). 1H NMR (400 MHz, CDCl3) δ ppm 8.69 (s, 1 H), 7.88 (d, J=9.32 Hz, 1 H), 7.43 (dd, J=9.32, 2.77 Hz, 1 H), 7.37 (d, J=2.77 Hz, 1 H), 3.95 (s, 3 H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07863291B2 |
| 出典データセット | uspto-grants-2011_01 |
| ORD ID | ord-25e0870ba1884210bdecf6b3e8813416 |
| 出典メモ | uspto-grants-2011_01 |