HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289182Generated: October 30, 2026
Acetic Acid → N-(2-cyano-3-methylbutanoyl)urea
https://huagongshe.com/reaction/2289182
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetone | HCID 180 | — |
| Reactant | Acetamide, N-(aminocarbonyl)-2-cyano- | HCID 74055 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2-cyano-3-methylbutanoyl)urea | HCID 9793952 | — |
Reaction Steps
Cyanoacetylurea (38.7 g) was suspended in N,N-dimethylformamide (77.4 ml), and acetone (24.6 ml), acetic acid (3.43 ml) and ammonium acetate (2.31 g) were added. This suspension was subjected to catalytic hydrogenation in the presence of 10% palladium carbon (0.78 g, 50% wet product) under normal pressure at 30° C. for 9 hours. The reaction mixture was heated to 70° C., and the catalyst was filtered off. Water (150 ml) was added to the filtrate to allow precipitation of crystals. The crystals were collected by filtration to give N-(2-cyano-3-methylbutanoyl)urea (yield 40.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090970 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-20bbf096ab37496f82b205653ee6a3c5 |
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| Source note | uspto-grants-2000_07 |
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