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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275893생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/275893

반응식

참여 물질

역할이름HCID투입량
반응물3-Ethoxy-4-methoxybenzaldehydeHCID 244728—
반응물beta-Alanine, ethyl ester, hydrochlorideHCID 458475—
반응물Sodium cyanoborohydrideHCID 5003444—
용매EthanolHCID 702—
생성물3-(3-Ethoxy-4-methoxy-benzylamino)-propionic acid ethyl esterHCID 5385854439.1%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06352977B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-63a853df8ade4b968ea2376812013b75
출처 메모uspto-grants-2002_03