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

HRID 2289182Notes

Reaction equation

HRID 2289182 reaction equation
[C:1]([CH2:3][C:4]([NH:6][C:7]([NH2:9])=[O:8])=[O:5])#[N:2].[CH3:10][C:11]([CH3:13])=O.C(O)(=O)C.C([O-])(=O)C.[NH4+]>CN(C)C=O.[C].[Pd]>[C:1]([CH:3]([CH:11]([CH3:13])[CH3:10])[C:4]([NH:6][C:7]([NH2:9])=[O:8])=[O:5])#[N:2]

Participants

7

Reactant 4

HCID 176Acetic AcidHCID 180AcetoneHCID 74055Acetamide, N-(aminocarbonyl)-2-cyano-HCID 517165Ammonium Acetate

Product 1

HCID 9793952N-(2-cyano-3-methylbutanoyl)urea

Reagents, catalysts & solvents 2

HCID 178418390HCID 178418390, compoundCatalystHCID 6228DimethylformamideSolvent

Conditions

Temperature
70 °C

Procedure

Cyanoacetylurea (38.7 g) was suspended in N,N-dimethylformamide (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 9 hours. The reaction mixture was heated to 70° C., 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 N-(2-cyano-3-methylbutanoyl)urea (yield 40.1 g).

Workup

  1. filtrationthe catalyst was filtered off
  2. additionWater (150 ml) was added to the filtrate
  3. customprecipitation of crystals
  4. filtrationThe crystals were collected by filtration

Sources & evidence

ORD record
ord-20bbf096ab37496f82b205653ee6a3c5
Source dataset
uspto-grants-2000_07
Patent number
US06090970

Reaction notes

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