Hydrogen Peroxide → HCID 14579257, compound

HRID 1975281Notes

Reaction equation

HRID 1975281 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][C:11](=[O:13])[CH3:12])=[CH:5][CH:4]=1)#[N:2].C(=O)(O)[O-:15].[K+].OO>CO.C(=O)([O-])[O-].[K+].[K+]>[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][C:11](=[O:13])[CH3:12])=[CH:5][CH:4]=1)(=[O:15])[NH2:2]

Participants

6

Reactant 3

HCID 784Hydrogen PeroxideHCID 516893Potassium BicarbonateHCID 112982374-(3-Oxobutyl)benzonitrile

Product 1

HCID 14579257HCID 14579257, compound

Reagents, catalysts & solvents 2

HCID 11430Potassium CarbonateCatalystHCID 887MethanolSolvent

Procedure

To a stirred solution of 9.70 g (0.056) mole of 4-(4-cyanophenyl)-2-butanone (the product of step (a)) in 15 ml of methanol, 1.80 g of potassium bicarbonate and 0.20 g of potassium carbonate were added. To the resulting mixture, 10.0 ml (0.088 mole) of 30% hydrogen peroxide was added dropwise over an hour. The reaction mixture was stirred for 24 hours and then chilled. The solid was collected by filtration, was rinsed twice with water and was dried to give 9.67 g of the above-identified product, melting point 152°-154° C. The 1H NMR was consistent with the assigned structure.

Workup

  1. temperaturechilled
  2. filtrationThe solid was collected by filtration
  3. washwas rinsed twice with water
  4. customwas dried

Sources & evidence

ORD record
ord-c0b35559799d4629aa2041d1699ae940
Source dataset
uspto-grants-1994_02
Patent number
US05286252

Reaction notes

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