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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 344892생성일: 2026년 10월 24일

Ethyl 3-ethoxy-3-iminopropionate hydrochloride → 2,3,4-trifluoro-N-[1-ethoxy-2-(ethoxycarbonyl)ethylidene]aniline

https://huagongshe.com/ko/reaction/344892

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참여 물질

역할이름HCID투입량
반응물Ethyl 3-ethoxy-3-iminopropionate hydrochlorideHCID 75345—
반응물2,3,4-TrifluoroanilineHCID 77468—
용매EthanolHCID 702—
생성물2,3,4-trifluoro-N-[1-ethoxy-2-(ethoxycarbonyl)ethylidene]anilineHCID 18641948105.5%

반응 조건

온도20 °C

반응 단계

2,3,4-Trifluoroaniline (58.8 g) is added in a single portion with stirring to a solution of 2-ethoxycarbonyl-1-ethoxyethylideneamine hydrochloride (90 g) in ethanol (820 cc). After 48 hours' stirring at a temperature in the region of 20° C., the suspension obtained is filtered; the filtrate is concentrated under reduced pressure (20 kPa) at a temperature in the region of 50° C. The oily residue is taken up with water (250 cc). The mixture obtained is extracted with ethyl ether (3×200 cc). The combined organic extracts are washed with water (4×150 cc), dried over magnesium sulphate and concentrated under reduced pressure (20 kPa) at approximately 30° C. 2,3,4-Trifluoro-N-[1-ethoxy-2-(ethoxycarbonyl)ethylidene]aniline (122 g) is obtained in the form of a yellow oil, which is used without further purification for the subsequent steps.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05053509
출처 데이터셋uspto-grants-1991_10
ORD IDord-9c008d3139064a119e4be92090e7f59b
출처 메모uspto-grants-1991_10