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化工社化工社 化学情報印刷レポート · 研究参考用
HRID 69045作成日:2026年10月23日

Hydrogen Peroxide → 3-Bromoquinolin-2-ol

https://huagongshe.com/ja/reaction/69045

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物Potassium CarbonateHCID 11430—
反応物3-BromoquinolineHCID 21413—
反応物Sodium SulfiteHCID 24437—
触媒HCID 178477782HCID 178477782—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物3-Bromoquinolin-2-olHCID 268338—

反応手順

Hydrogen peroxide solution (5.9 ml) was added to a THF solution (16 ml) of methyltrioxorhenium (VII) (24 mg). The mixture was stirred for 10 minutes at room temperature. 3-Bromoquinoline (4.0 g) was added thereto, and the mixture was stirred at room temperature for four days. Ethyl acetate (20 ml) was added to the reaction mixture. 20% Sodium sulfite aqueous solution (30 ml) was added slowly to the mixture under ice cooling. The mixture was stirred at room temperature. The organic layer was condensed to a half volume under reduced pressure. Ethyl acetate (20 ml) and 15% potassium carbonate aqueous solution (19 ml) were added thereto, and the organic layer was extracted. 15% Potassium carbonate aqueous solution (19 ml) of p-toluenesulfonyl chloride (4 g) were added thereto. The mixture was stirred for 10 minutes at room temperature. The generated insoluble matter was separated, washed with ethyl acetate, water, and then with ether, and dried to give the title compound (3.2 g) as a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822453B2
出典データセットuspto-grants-2014_09
ORD IDord-4619ec1e0624416bb44eb940d1a9c089
出典メモuspto-grants-2014_09