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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 622704생성일: 2026년 10월 26일

Dimethylformamide → 1-(3-Methoxy-2-nitro-6-methylpyridylmethyl)-2-nitromethyleneimidazolidine

https://huagongshe.com/reaction/622704

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물2-(Nitromethylene)imidazolidineHCID 3014763—
반응물3-Methoxy-2-nitro-6-pyridylmethyl bromideHCID 14405124—
반응물HCID 178418361HCID 178418361—
생성물1-(3-Methoxy-2-nitro-6-methylpyridylmethyl)-2-nitromethyleneimidazolidineHCID 86742440—

반응 조건

온도60 °C

반응 단계

Nitromethyleneimidazolidine (1.3 g) was dissolved in dry dimethylformamide (15 ml), and sodium hydride (0.26 g) was added. The mixture was stirred at room temperature until the generation of hydrogen ceased. Subsequently, a solution of 2.4 g of 3-methoxy-2-nitro-6-pyridylmethyl bromide in 5 ml of dimethylformamide was added, and the mixture was stirred at 60° C. for 15 minutes. The reaction mixture was cooled to room temperature, poured into 50 ml of ice water, and extracted with dichloromethane. Dichloromethane was distilled off under reduced pressure, and ethanol was added to the residue to precipitate crystals. The crystals were collected by filtration and washed with ethanol to give 1-(3-methoxy-2-nitro-6-methylpyridylmethyl)-2-nitromethyleneimidazolidine (0.4 g). mp. 177°-181° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04772620
출처 데이터셋uspto-grants-1988_09
ORD IDord-4cdc866464844c1c9043c9b082818713
출처 메모uspto-grants-1988_09