Hydrochloric Acid → HCID 178515568, compound
Reaction equation
[O:1]=[C:2]1[CH:7]=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[O:5][C:4]([C:14]#[N:15])=[CH:3]1.[N-:16]=[N+:17]=[N-:18].[Na+].[Cl-].[NH4+].Cl>CN(C)C=O>[C:8]1([C:6]2[O:5][C:4]([C:14]3[NH:18][N:17]=[N:16][N:15]=3)=[CH:3][C:2](=[O:1])[CH:7]=2)[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 4-oxo-6-phenyl-4H-pyran-2-carbonitrile (1.10 g), sodium azide (0.45 g) and ammonium chloride (0.37 g) in dry dimethylformamide (10 ml) was stirred at room temperature for 2 hours. A precipitate formed. Dilute hydrochloric acid (1 M, 20 ml) was added and the resulting white solid was filtered off. Recrystallisation from acetic acid yielded the title product as white crystals (251°-254° C. with decomposition).
Workup
- customA precipitate formed
- filtrationthe resulting white solid was filtered off
- customRecrystallisation from acetic acid
Sources & evidence
- ORD record
- ord-be94c9cffa194cdbbbd58e39e373b89f
- Source dataset
- uspto-grants-1984_05
- Patent number
- US04448787
Reaction notes
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