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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289187Generated: October 30, 2026

Acetic Acid → N-(2-cyano-3-methylbutanoyl)urea

https://huagongshe.com/reaction/2289187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetamide, N-(aminocarbonyl)-2-cyano-HCID 74055—
ReactantAmmonium AcetateHCID 517165—
CatalystHCID 178418390HCID 178418390—
SolventAcetoneHCID 180—
ProductN-(2-cyano-3-methylbutanoyl)ureaHCID 9793952889.9%

Reaction Steps

Cyanoacetylurea (51.6 g) was suspended in acetone (516 ml), and acetic acid (4.8 g) and ammonium acetate (3.2 g) were added. This suspension was subjected to catalytic hydrogenation in the presence of 5% palladium carbon (4.1 g, 50% wet product) under normal pressure at 40° C. for 5 hours. The reaction mixture was refluxed under heating to dissolve an insoluble matter, and the catalyst was filtered off. The obtained filtrate was concentrated to a half, and water (258 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 62.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090970
Source datasetuspto-grants-2000_07
ORD IDord-0f0102f8891444c7bf276eecf94c4356
Source noteuspto-grants-2000_07