Phosphorus oxychloride → HCID 73679007, compound
Reaction equation
[S:1]([C:5]1[CH:14]=[CH:13][C:12]([NH:15][N:16]=[C:17]([C:20]([CH3:22])=[O:21])[C:18]#[N:19])=[C:11]2[C:6]=1[CH:7]=[CH:8][CH:9]=[N:10]2)(O)(=[O:3])=[O:2].[K].P(Cl)(Cl)([Cl:26])=O>CN1CCCC1=O>[Cl:26][S:1]([C:5]1[CH:14]=[CH:13][C:12]([NH:15][N:16]=[C:17]([C:20]([CH3:22])=[O:21])[C:18]#[N:19])=[C:11]2[C:6]=1[CH:7]=[CH:8][CH:9]=[N:10]2)(=[O:3])=[O:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a 250 ml round-bottom flask fitted with calcium sulfate drying tube was added 4.5 g (0.0126 m) of 2-(5-sulfo-8-quinolylhydrazono)acetoacetonitrile, potassium salt and 45 ml phosphorus oxychloride. The resultant slurry was chilled to <5° C. and 4.5 ml N-methylpyrrolidinone was slowly added. After stirring 1 hour. at 0°-5° C., the slurry was stirred overnight at room temperature followed by quenching in 500 ml ice water. The resultant yellow solid was collected, air dried and recrystallized from 100 ml acetonitrile. Yield 3.0 g yellow needles (70 percent).
Workup
- customTo a 250 ml round-bottom flask fitted with calcium sulfate drying tube
- temperatureThe resultant slurry was chilled to <5° C.
- stirringat 0°-5° C., the slurry was stirred overnight at room temperature
- customby quenching in 500 ml ice water
- customThe resultant yellow solid was collected
- customair dried
- customrecrystallized from 100 ml acetonitrile
Sources & evidence
- ORD record
- ord-aef72aaa55d24866bd571194720397fc
- Source dataset
- uspto-grants-1983_11
- Patent number
- US04418131
Reaction notes
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