Acetic Acid → HCID 367454, compound
Reaction equation
[N+:1]([C:4]1[CH:11]=[CH:10][C:7]([CH:8]=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].[C:12]([CH2:15][C:16](=[O:18])[CH3:17])(=[O:14])[CH3:13].N1CCCCC1.C(O)(=O)C>C(O)(C)C>[N+:1]([C:4]1[CH:11]=[CH:10][C:7]([CH:8]=[C:15]([C:16](=[O:18])[CH3:17])[C:12](=[O:14])[CH3:13])=[CH:6][CH:5]=1)([O-:3])=[O:2]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
30.2 g (0.2 mol) of 4-nitrobenzaldehyde and 30.0 g (0.3 mol) of acetylacetone are dissolved in 200 ml of isopropanol and treated with 1.2 ml of piperidine and 1 ml of glacial acetic acid. The mixture is warmed in a water bath until a clear solution is formed and then stirred at RT for 4 h. The product precipitates and is filtered off with suction.
Workup
- temperatureThe mixture is warmed in a water bath until a clear solution
- customis formed
- customThe product precipitates
- filtrationis filtered off with suction
Sources & evidence
- ORD record
- ord-a570f78df2fc4530abca2a69c8ff7e55
- Source dataset
- uspto-grants-2000_11
- Patent number
- US06147087
Reaction notes
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