Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetoneHCID 180—
ReactantAcetamide, N-(aminocarbonyl)-2-cyano-HCID 74055—
ReactantAmmonium AcetateHCID 517165—
CatalystHCID 178418390HCID 178418390—
SolventDimethylformamideHCID 6228—
ProductN-(2-cyano-3-methylbutanoyl)ureaHCID 979395285.7%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090970
Source datasetuspto-grants-2000_07
ORD IDord-7b78d784562747a4a8328ce3996de126
Source noteuspto-grants-2000_07