Sodium Hydroxide → HCID 178509267, compound
Reaction equation
C[N:2]([CH:4]=[C:5]([C:8](=[O:15])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:6]#[N:7])C.[N+:16]([O-])(O)=O.NNC(N)=N.[OH-].[Na+]>C(O)C>[NH2:2][C:4]1[C:5]([C:8]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[O:15])=[CH:6][NH:7][N:16]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A reaction mixture comprisng 73.36 g of α-[(dimethylamino)methylene]-β-oxo-2-benzenepropanenitrile, 63.45 g of aminoguanidine nitrate, 500 ml of ethanol and 36.6 ml of 10N sodium hydroxide was refluxed for 10 hours and then cooled. The resulting precipitate was collected and washed with water, giving 17.1 g of the desired product, mp 177°-179° C.
Workup
- temperaturecooled
- customThe resulting precipitate was collected
- washwashed with water
Sources & evidence
- ORD record
- ord-ecb6dd84699b48ab807954f0301761d6
- Source dataset
- uspto-grants-1990_02
- Patent number
- US04900836
Reaction notes
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