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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 648970생성일: 2026년 10월 24일

3-(7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-on-3-yl)-propionaldehyde diethylacetal → 3-(7,8-dimethoxy-2-oxo-1,2-dihydro-3H-benzo[d]azepin-3-yl)propanal

https://huagongshe.com/ko/reaction/648970

반응식

참여 물질

역할이름HCID투입량
반응물3-(7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-on-3-yl)-propionaldehyde diethylacetalHCID 13579643—
용매EthanolHCID 702—
용매Sulfuric AcidHCID 1118—
생성물3-(7,8-dimethoxy-2-oxo-1,2-dihydro-3H-benzo[d]azepin-3-yl)propanalHCID 13579661—

반응 조건

온도40 °C

반응 단계

Here, 3-(7,8-dimethoxy-1,3-dihydro-2H-3-benzazepin-2-on-3-yl)-propionaldehyde diethylacetal (3.5 g, 0.01 mol) is heated to 40° C. for 2 hours in 2N sulphuric acid (50 ml) and ethanol (50 ml). The alcohol is distilled off in vacuo, the residue is made alkaline with saturated potassium carbonate solution while cooling and extracted several times with ethyl acetate. The ethyl acetate extract is extracted twice with 5% sodium hydrogen sulfate solution. The bisulphate extract is acidified with concentrated hydrochloric acid and heated to 40° C. in vacuo for half an hour to eliminate the sulphur dioxide. Then saturated potassium carbonate solution is added, the mixture is extracted several times with methylene chloride, dried over magnesium sulphate and concentrated by evaporation.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04737495
출처 데이터셋uspto-grants-1988_04
ORD IDord-36540b6089e04859b72fe8cb68eb3645
출처 메모uspto-grants-1988_04