Oxygen → HCID 21393982, compound
Reaction equation
[CH:1]1([NH:7][N:8]=[C:9]([CH3:11])[CH3:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[O:12]=[O:13]>CCCCCCC>[CH:1]1([N:7]=[N:8][C:9]([O:12][OH:13])([CH3:11])[CH3:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 5.0 grams (0.0324 moles) of acetone cyclohexylhydrazone in 70 grams of heptane was oxidized by passing oxygen through the solution as in Example II. The oxidation was initiated at 35° C. The reaction was followed by gas chromatography, following the disappearance of the cyclohexylhydrazone peak. The reaction was complete in 35 minutes at 35° C. The solution was cooled to 0° and drained into a tared, cooled, polyethylene bottle, weighed and stored at -30° C. The solution weighed 75.1 grams (85% yield).
Workup
- customwas initiated at 35° C
- temperatureThe solution was cooled to 0°
- temperaturecooled
- customstored at -30° C
Sources & evidence
- ORD record
- ord-f071b4d560284213954c0812e78978fa
- Source dataset
- uspto-grants-1977_12
- Patent number
- US04063012
Reaction notes
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