Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 972212생성일: 2026년 10월 24일
Dimethylformamide → Methyl(1-((2,4-dichlorphenoxy)acetyl)-3-methyl-2-imidazolidinylidene)nitroacetate
https://huagongshe.com/ko/reaction/972212
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | (2,4-Dichlorophenoxy)acetyl chloride | HCID 69887 | — |
| 반응물 | (1-Methyl-2-imidazolidinylidene)nitroacetic acid | HCID 86735005 | — |
| 생성물 | Methyl(1-((2,4-dichlorphenoxy)acetyl)-3-methyl-2-imidazolidinylidene)nitroacetate | HCID 54513855 | — |
반응 단계
2.3 g of sodium hydride was slurried in 75 ml of dimethylformamide at 5°. To that slurry, at 5°, was added 19.5 g of 1B over a 30-minute period. The stirred mixture was allowed to warm to room temperature and stirred at that temperature for one hour. The mixture then was cooled to 5° and there was added thereto a solution of 25.5 g of 2,4-dichlorophenoxyacetyl chloride in 25 ml of dimethylformamide, over a 20-minute period, the stirred mixture being held at 5°-12°. The stirred mixture was allowed to warm to room temperature and stirred at that temperature overnight. The mixture then was poured into ice water. The solid was filtered, washed with water and dried by air aspiration and ether washing to give a tan-colored solid, which on recrystallization from acetonitrile gave 1, as an off-white solid, m.p.; 191°-192° (with decomposition).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04052411 |
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| 출처 데이터셋 | uspto-grants-1977_10 |
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| ORD ID | ord-23f428c50188440e862d78e2954b53b6 |
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| 출처 메모 | uspto-grants-1977_10 |
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