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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl 3-ethoxy-3-iminopropionate hydrochloride | HCID 75345 | — |
| 반응물 | 2,3,4-Trifluoroaniline | HCID 77468 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 2,3,4-trifluoro-N-[1-ethoxy-2-(ethoxycarbonyl)ethylidene]aniline | HCID 18641948 | 105.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05053509 |
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| 출처 데이터셋 | uspto-grants-1991_10 |
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| ORD ID | ord-9c008d3139064a119e4be92090e7f59b |
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| 출처 메모 | uspto-grants-1991_10 |
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