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HRID 39689作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物2-HydroxyquinolineHCID 6038—
反応物DimethylformamideHCID 6228—
反応物Sodium hydrideHCID 24758—
反応物1,3-Dioxolane, 2-(bromomethyl)-HCID 78068—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物1-(1,3-dioxolan-2-ylmethyl)quinolin-2(1H)-oneHCID 59397864—

反応条件

温度52.5 °C

反応手順

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.

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-1482b7112e89491d827b644a08da0031
出典メモuspto-grants-2013_09