化工社化工社 化学情報印刷レポート · 研究参考用
Tetradecyltrimethylammonium → 2,2-Bis(5-chloro-pyrid-2-yl)oxirane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetradecyltrimethylammonium | HCID 14251 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| 反応物 | Bis(5-chloropyridin-2-yl)methanone | HCID 20274519 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | 1,1,1-Trichloroethane | HCID 6278 | — |
| 生成物 | 2,2-Bis(5-chloro-pyrid-2-yl)oxirane | HCID 20274520 | — |
反応手順
A mixture of bis-(5-chloropyrid-2-yl)ketone (0.8 g), trimethylsulphoxonium iodide (0.84 g), cetrimide (0.08 g) and sodium hydroxide (3 g) in water (16 ml) and 1,1,1-trichloroethane (30 ml) was stirred vigorously and heated at 70° to 75° C. for 2.5 hours. Further trimethylsulphoxonium iodide (0.86 g) was added and the mixture heated at 75° to 80° C. for a further 2 hours. The mixture was cooled, diluted with water (10 ml) and extracted with dichloromethane (3×20 ml). The combined organic extracts were dried over magnesium sulfate and evaporated to yield the crude title compound as a brownish paste (0.8 g), which was used directly.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04529799 |
| 出典データセット | uspto-grants-1985_07 |
| ORD ID | ord-60f7680d16274171ac481390664b83f4 |
| 出典メモ | uspto-grants-1985_07 |