Phosphorus oxychloride → HCID 73679007, compound

HRID 1649568Notes

Reaction equation

HRID 1649568 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

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

  1. customTo a 250 ml round-bottom flask fitted with calcium sulfate drying tube
  2. temperatureThe resultant slurry was chilled to <5° C.
  3. stirringat 0°-5° C., the slurry was stirred overnight at room temperature
  4. customby quenching in 500 ml ice water
  5. customThe resultant yellow solid was collected
  6. customair dried
  7. 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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