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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

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물(2,4-Dichlorophenoxy)acetyl chlorideHCID 69887—
반응물(1-Methyl-2-imidazolidinylidene)nitroacetic acidHCID 86735005—
생성물Methyl(1-((2,4-dichlorphenoxy)acetyl)-3-methyl-2-imidazolidinylidene)nitroacetateHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04052411
출처 데이터셋uspto-grants-1977_10
ORD IDord-23f428c50188440e862d78e2954b53b6
출처 메모uspto-grants-1977_10