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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2193126생성일: 2026년 10월 26일

Hydrochloric Acid → 4-Acetyl-1-(1,3-dioxolan-2-ylmethyl)-2-oxo-3,4-dihydro-1h-quinoxaline

https://huagongshe.com/reaction/2193126

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물1,3-Dioxolane, 2-(bromomethyl)-HCID 78068—
반응물4-Acetyl-3,4-dihydroquinoxalin-2(1H)-oneHCID 2770825—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물4-Acetyl-1-(1,3-dioxolan-2-ylmethyl)-2-oxo-3,4-dihydro-1h-quinoxalineHCID 59398159—

반응 단계

To 15 mL of an N,N-dimethylformamide solution containing 957 mg of 4-acetyl-3,4-dihydro-2-oxo-1H-quinoxaline, 668 mg of sodium hydride was added, and the mixture was stirred at room temperature for 1 hour. Thereto was added 2.6 mL of 2-bromomethyl-1,3-dioxolane, and the mixture was stirred at 90° C. for 6 hours. The reaction mixture was cooled to room temperature, and then ethyl acetate and 1 mol/L hydrochloric acid were added thereto. The organic layer was separated, washed sequentially with water and 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; Silica gel 60 manufactured by Kanto Chemical Co., Inc., eluent; chloroform] to obtain 1.30 g of a brown oily substance, 4-acetyl-1-(1,3-dioxolan-2-ylmethyl)-2-oxo-3,4-dihydro-1H-quinoxaline.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08329694B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-b9aeda3f88744744bf8f74b7be62b48f
출처 메모uspto-grants-2012_12