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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Ethoxy-4-methoxybenzaldehyde | HCID 244728 | — |
| 반응물 | beta-Alanine, ethyl ester, hydrochloride | HCID 458475 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 3-(3-Ethoxy-4-methoxy-benzylamino)-propionic acid ethyl ester | HCID 53858544 | 39.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06352977B1 |
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| 출처 데이터셋 | uspto-grants-2002_03 |
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| ORD ID | ord-63a853df8ade4b968ea2376812013b75 |
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| 출처 메모 | uspto-grants-2002_03 |
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