Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27681생성일: 2026년 10월 25일
Formamide → Acetamide, N-(2-(2-(2-cyano-4,6-dinitrophenyl)diazenyl)-5-(diethylamino)phenyl)-
https://huagongshe.com/reaction/27681
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Formamide | HCID 713 | — |
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Acetamide, N-[2-[2-(2-bromo-4,6-dinitrophenyl)diazenyl]-5-(diethylamino)phenyl]- | HCID 104287 | — |
| 반응물 | Sodium Acetate | HCID 517045 | — |
| 촉매 | Cupric Chloride | HCID 24014 | — |
| 용매 | Butyl Acetate | HCID 31272 | — |
| 생성물 | Acetamide, N-(2-(2-(2-cyano-4,6-dinitrophenyl)diazenyl)-5-(diethylamino)phenyl)- | HCID 90383 | 96% |
반응 단계
2-Bromo-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene (2.4 parts), copper (II) chloride (0.67 parts), anhydrous sodium acetate (1.2 parts), formamide (1.8 parts), acetic anhydride (2.0 parts) and n-butyl acetate (44 parts) are mixed together and heated, with stirring, to 110° C. during 15 minutes. The temperature is maintained for 5 hours after which time the reaction is complete. The mixture is cooled to room temperature and poured into petroleum-ether (boiling range 60-80°) (400 parts). The precipitate is collected, washed with petroleum-ether (100 parts) and dried. 2-Cyano-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene is obtained in 96% yield.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04222935 |
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| 출처 데이터셋 | uspto-grants-1980_09 |
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| ORD ID | ord-a9221bcf0bbb4c9692966241d39232ec |
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| 출처 메모 | uspto-grants-1980_09 |
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