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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetoneHCID 180—
ReactantAcetamide, N-(aminocarbonyl)-2-cyano-HCID 74055—
ReactantAmmonium AcetateHCID 517165—
CatalystHCID 178418390HCID 178418390—
SolventIsopropanolHCID 3776—
ProductN-(2-cyano-3-methylbutanoyl)ureaHCID 9793952—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090970
Source datasetuspto-grants-2000_07
ORD IDord-89700ca4f9024da8a5130b4da667becb
Source noteuspto-grants-2000_07