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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39734생성일: 2026년 10월 23일

Hydrochloric Acid → 1-(1,3-Dioxolan-2-ylmethyl)-8-methylquinolin-2(1h)-one

https://huagongshe.com/ko/reaction/39734

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물1,3-Dioxolane, 2-(bromomethyl)-HCID 78068—
반응물8-methylquinolin-2(1H)-oneHCID 5325167—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물1-(1,3-Dioxolan-2-ylmethyl)-8-methylquinolin-2(1h)-oneHCID 59398217—

반응 단계

To 3 mL of an N,N-dimethylformamide solution containing 0.17 g of 8-methylquinolin-2(1H)-one, 0.13 g of 60% sodium hydride was added under a nitrogen atmosphere, and the mixture was stirred at room temperature for 30 minutes. Thereto was added 0.89 g of 2-bromomethyl-1,3-dioxolane, and the mixture was stirred at 90° C. for 48 hours. The reaction mixture was cooled to room temperature, then ethyl acetate and 1 mol/L hydrochloric acid were added thereto. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate. 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. The residue thus obtained was purified by silica gel column chromatography [silica gel; Chromatorex-NH, manufactured by Fuji Silysia Chemical Ltd., eluent; hexane:ethyl acetate=8:1] to obtain 0.18 g of a pale yellow oily substance, 1-(1,3-dioxolan-2-ylmethyl)-8-methylquinolin-2(1H)-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524738B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-5f873118b5a743369c8e20d0ff654f65
출처 메모uspto-grants-2013_09