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HRID 39730作成日:2026年10月24日

4-Chloro-7-(trifluoromethyl)quinoline → 4-Chloro-1-oxo-7-(trifluoromethyl)-1lambda~5~-quinoline

https://huagongshe.com/ja/reaction/39730

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-7-(trifluoromethyl)quinolineHCID 67668—
反応物m-Chloroperbenzoic acidHCID 70297—
反応物Sodium BicarbonateHCID 516892—
溶媒ChloroformHCID 6212—
生成物4-Chloro-1-oxo-7-(trifluoromethyl)-1lambda~5~-quinolineHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524738B2
出典データセットuspto-grants-2013_09
ORD IDord-0c9d7f38499840a9bd74ad95e8a955b4
出典メモuspto-grants-2013_09