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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1380866생성일: 2026년 10월 27일

Ethanol → 3-(7,8-dimethoxy-2-oxo-1,2-dihydro-3H-benzo[d]azepin-3-yl)propanal

https://huagongshe.com/reaction/1380866

반응식

참여 물질

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

반응 단계

First, 3-(7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-on-3-yl)-propionaldehyde diethyl acetal (3.5 g, 0.01 mol) is heated in 2N sulphuric acid (50 ml) and ethanol (50 ml) to 40° C. for 2 hours. The alcohol is then distilled off in vacuo, the residue is made alkaline with saturated potassium carbonate solution with cooling and extracted several times with ethyl acetate. The ethyl acetate extract is extracted twice with sodium hydrogensulphite solution. The bisulphite extract is acidified with concentrated hydrochloric acid and heated for half an hour to 40° C. in vacuo in order to eliminate the sulphur dioxide. Then, saturated potassium carbonate solution is added and the mixture is extracted several times with methylene chloride, dried over magnesium sulphate and evaporated. Yield: 1.7 g. Mp: 95°-96° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04584293
출처 데이터셋uspto-grants-1986_04
ORD IDord-7c522c6de0974f9ea436431392b948db
출처 메모uspto-grants-1986_04