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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39689생성일: 2026년 10월 23일

2-Hydroxyquinoline → 1-(1,3-dioxolan-2-ylmethyl)quinolin-2(1H)-one

https://huagongshe.com/ko/reaction/39689

반응식

참여 물질

역할이름HCID투입량
반응물2-HydroxyquinolineHCID 6038—
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물1,3-Dioxolane, 2-(bromomethyl)-HCID 78068—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물1-(1,3-dioxolan-2-ylmethyl)quinolin-2(1H)-oneHCID 59397864—

반응 조건

온도52.5 °C

반응 단계

To 11.5 mL of an N,N-dimethylformamide solution containing 1.15 g of quinolin-2(1H)-one, 0.35 g of 60% sodium hydride was added, and the mixture was stirred at 50 to 55° C. for 20 minutes. Thereto was added 0.90 mL of 2-bromomethyl-1,3-dioxolane, and the reaction mixture was stirred at 85 to 95° C. for 30 minutes. The reaction mixture was further added with 0.35 g of 60% sodium hydride and 0.90 mL of 2-bromomethyl-1,3-dioxolane, and stirred for 1 hour. The mixture was further added with 0.35 g of 60% sodium hydride and 0.90 mL of 2-bromomethyl-1,3-dioxolane, and stirred for 1 hour and 30 minutes. The reaction mixture was cooled to room temperature, and then water and ethyl acetate were added thereto. The organic layer was separated, and the aqueous layer was extracted twice with ethyl acetate. The organic layer and the extract were combined, the resultant solution was washed with a saturated sodium chloride solution and dried over anhydrous magnesium sulfate, the solvent was removed under reduced pressure, and the residue thus obtained was purified by silica gel column chromatography [eluent; hexane:ethyl acetate 2:1] to obtain 0.89 g of a yellow oily substance, 1-(1,3-dioxolan-2-ylmethyl)quinolin-2(1H)-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524738B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-1482b7112e89491d827b644a08da0031
출처 메모uspto-grants-2013_09