Peracetic Acid → HCID 86737265, compound
Reaction equation
[C:1]([N:5]=[N:6][C:7]([O:10][CH3:11])([CH3:9])[CH3:8])([CH3:4])([CH3:3])[CH3:2].C(OO)(=[O:14])C>C(OCC)(=O)C>[C:1]([N+:5](=[N:6][C:7]([O:10][CH3:11])([CH3:9])[CH3:8])[O-:14])([CH3:4])([CH3:3])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2-t-Butylazoxy-2-methoxypropane was prepared by oxidizing 7.9 grams (0.05 moles) 2-t-butylazo-2-methoxypropane with 50 ml. of 25% peracetic acid in ethyl acetate at 30°-40° C. for 2 hours. The yield was 7.3 grams (84% yield) of a colorless liquid. The infrared spectrum of the product was in agreement with the structure of 2-t-butylazoxy-2-methoxypropane (2 strong bands at 1450-1510 cm-1).
Sources & evidence
- ORD record
- ord-d9257e02b8dd4a46aa98d6119f0b8728
- Source dataset
- uspto-grants-1980_10
- Patent number
- US04228069
Reaction notes
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