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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 2-(Nitromethylene)imidazolidine | HCID 3014763 | — |
| 반응물 | 3-Methoxy-2-nitro-6-pyridylmethyl bromide | HCID 14405124 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 생성물 | 1-(3-Methoxy-2-nitro-6-methylpyridylmethyl)-2-nitromethyleneimidazolidine | HCID 86742440 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04772620 |
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| 출처 데이터셋 | uspto-grants-1988_09 |
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| ORD ID | ord-4cdc866464844c1c9043c9b082818713 |
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| 출처 메모 | uspto-grants-1988_09 |
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