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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69045생성일: 2026년 10월 23일

Hydrogen Peroxide → 3-Bromoquinolin-2-ol

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물Potassium CarbonateHCID 11430—
반응물3-BromoquinolineHCID 21413—
반응물Sodium SulfiteHCID 24437—
촉매HCID 178477782HCID 178477782—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물3-Bromoquinolin-2-olHCID 268338—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822453B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-4619ec1e0624416bb44eb940d1a9c089
출처 메모uspto-grants-2014_09