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HRID 1380866作成日:2026年10月27日

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

https://huagongshe.com/reaction/1380866

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物3-(7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-on-3-yl)-propionaldehyde diethylacetalHCID 13579643—
溶媒Sulfuric AcidHCID 1118—
生成物3-(7,8-dimethoxy-2-oxo-1,2-dihydro-3H-benzo[d]azepin-3-yl)propanalHCID 13579661—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04584293
出典データセットuspto-grants-1986_04
ORD IDord-7c522c6de0974f9ea436431392b948db
出典メモuspto-grants-1986_04