HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289184Generated: October 31, 2026
Acetic Acid → N-(2-cyano-3-methylbutanoyl)urea
https://huagongshe.com/reaction/2289184
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 | Isopropanol | HCID 3776 | — |
| Product | N-(2-cyano-3-methylbutanoyl)urea | HCID 9793952 | — |
Reaction Steps
Cyanoacetylurea (38.7 g) was suspended in isopropanol (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 8 hours. The reaction mixture was heated to 80° C. for 1 hour, 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 crystals of N-(2-cyano-3-methylbutanoyl)urea (yield 21.7 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-89700ca4f9024da8a5130b4da667becb |
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| Source note | uspto-grants-2000_07 |
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