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HRID 275893作成日:2026年10月27日

3-Ethoxy-4-methoxybenzaldehyde → 3-(3-Ethoxy-4-methoxy-benzylamino)-propionic acid ethyl ester

https://huagongshe.com/reaction/275893

反応式

関与物質

役割名称HCID仕込み量
反応物3-Ethoxy-4-methoxybenzaldehydeHCID 244728—
反応物beta-Alanine, ethyl ester, hydrochlorideHCID 458475—
反応物Sodium cyanoborohydrideHCID 5003444—
溶媒EthanolHCID 702—
生成物3-(3-Ethoxy-4-methoxy-benzylamino)-propionic acid ethyl esterHCID 5385854439.1%

反応手順

A mixture of β-alanine ethyl ester hydrochloride (1.6 g), 3-ethoxy-4-methoxybenzaldehyde (1.8 g), sodium cyanoborohydride (0.42 g) and powdered 3Å molecular seives (2.5 g) in ethanol (25 ml) was stirred at ambient temperature for 24 hours. A further aliquot of sodium cyanoborohydride (0.42 g) was added and stirring was continued for a further 24 hours. The reaction mixture was filtered and the filtrate was evaporated. The residue was treated with ethyl acetate (100 ml) and the solution was washed with 10% aqueous potassium carbonate (50 ml), then twice with water (25 ml), then with brine (25 ml), then dried over magnesium sulphate and then evaporated. The residual oil was subjected to flash chromatography on silica eluting with a mixture of dichloromethane and methanol (95:5, v/v) to give the title compound as a colourless oil (1.1 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06352977B1
出典データセットuspto-grants-2002_03
ORD IDord-63a853df8ade4b968ea2376812013b75
出典メモuspto-grants-2002_03