HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289186Generated: October 31, 2026
Acetic Acid → N-(2-cyano-3-methylbutanoyl)urea
https://huagongshe.com/reaction/2289186
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 | 85.7% |
Reaction Steps
Cyanoacetylurea (78.6 g) was suspended in N,N-dimethylformamide (154.9 ml), and acetone (48.8 g), acetic acid (7.2 g) and ammonium acetate (4.6 g) were added. This suspension was subjected to catalytic hydrogenation in the presence of 10% palladium carbon (3.1 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. to dissolve an insoluble matter, and the catalyst was filtered off. Water (390 ml) was added to the obtained filtrate to allow precipitation of crystals. The crystals were collected by filtration to give crystals of N-(2-cyano-3-methylbutanoyl)urea (yield 89.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06090970 |
|---|
| Source dataset | uspto-grants-2000_07 |
|---|
| ORD ID | ord-7b78d784562747a4a8328ce3996de126 |
|---|
| Source note | uspto-grants-2000_07 |
|---|