HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27681Generated: October 25, 2026
Formamide → Acetamide, N-(2-(2-(2-cyano-4,6-dinitrophenyl)diazenyl)-5-(diethylamino)phenyl)-
https://huagongshe.com/reaction/27681
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formamide | HCID 713 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Acetamide, N-[2-[2-(2-bromo-4,6-dinitrophenyl)diazenyl]-5-(diethylamino)phenyl]- | HCID 104287 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Butyl Acetate | HCID 31272 | — |
| Product | Acetamide, N-(2-(2-(2-cyano-4,6-dinitrophenyl)diazenyl)-5-(diethylamino)phenyl)- | HCID 90383 | 96% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04222935 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-a9221bcf0bbb4c9692966241d39232ec |
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| Source note | uspto-grants-1980_09 |
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