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Phosphorus oxychloride → 3-Chloropyridine-4-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Phosphorus oxychloride | HCID 24813 | — |
| 反応物 | Phosphorus pentachloride | HCID 24819 | — |
| 反応物 | 4-Pyridinecarbonitrile, 1-oxide | HCID 84684 | — |
| 生成物 | 2-Chloro-4-cyanopyridine | HCID 568638 | 24% |
| 生成物 | 3-Chloropyridine-4-carbonitrile | HCID 10678306 | 30% |
反応手順
A mixture of 4-cyanopyridine N-oxide (30 g, 0.25 mol), phosphorous oxychloride (96 ml, 0.35 mol) and phosphorous pentachloride (72 g, 0.38 mol) was refluxed at 120°-130° C. for 6 hours and then stirred at room temperature for 12 hours. The reaction mixture was slowly poured into a mixture of ice/Na2CO3 /K2CO3 and was extracted with chloroform (4×250 ml). The solvent was removed in vacuo and the residue was purified by column chromatography on silica eluting with 50% ether/hexanes to afford 8.4 g (24%) of 2-chloro-4-cyanopyridine, m.p. 69.5°-70.5° C. and 10.5 g (30%) of 3-chloro-4-cyanopyridine, m.p. 71.5°-72° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05541187 |
| 出典データセット | uspto-grants-1996_07 |
| ORD ID | ord-a76b0051cb7a4357aedaa7d94e168dfa |
| 出典メモ | uspto-grants-1996_07 |