化工社化工社 化学情報印刷レポート · 研究参考用
4-Chloro-7-(trifluoromethyl)quinoline → 4-Chloro-1-oxo-7-(trifluoromethyl)-1lambda~5~-quinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Chloro-7-(trifluoromethyl)quinoline | HCID 67668 | — |
| 反応物 | m-Chloroperbenzoic acid | HCID 70297 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 4-Chloro-1-oxo-7-(trifluoromethyl)-1lambda~5~-quinoline | HCID 23128133 | — |
反応手順
To 14 mL of a chloroform solution containing 0.90 g of 4-chloro-7-trifluoromethylquinoline, 1.04 g of m-chloroperbenzoic acid was added, and the mixture was stirred at room temperature for 3.5 hours. The reaction mixture was added with 15 mL of an aqueous saturated sodium hydrogen carbonate solution. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, the resultant solution was washed with an aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain a yellow solid, 4-chloro-7-trifluoromethylquinoline N-oxide.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08524738B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-0c9d7f38499840a9bd74ad95e8a955b4 |
| 出典メモ | uspto-grants-2013_09 |