HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289183Generated: October 30, 2026
Acetic Acid → N-(2-cyano-3-methylbutanoyl)urea
https://huagongshe.com/reaction/2289183
Participants
| Role | Name | HCID | Charge |
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| 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 (116.1 g) was suspended in N,N-dimethylformamide (219.3 ml), and acetone (73.1 ml), acetic acid (10.8 ml) and ammonium acetate (6.93 g) were added. This suspension was subjected to catalytic hydrogenation in the presence of 10% palladium carbon (2.33 g, 50% wet product) under hydrogen pressure at 10 kg/cm2 and at 25° C. for 4 hours. The reaction mixture was heated to 70° C., and the catalyst was filtered off. Water (745 ml) was added to the filtrate to allow precipitation of crystals. The crystals were collected by filtration to give crystals of N-(2-cyano-3-methylbutanoyl)urea (yield 134.5 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-12218aa0d0f64c949def3be4b2200f14 |
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| Source note | uspto-grants-2000_07 |
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