Dimethylamine → HCID 53665727, compound
Reaction equation
[CH3:1][N:2]([C:11](SC)=[C:12]([C:15]#[N:16])[C:13]#[N:14])[N:3]=[CH:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[CH3:19][NH:20][CH3:21]>C(O)C>[CH3:1][N:2]([C:11]([N:20]([CH3:21])[CH3:19])=[C:12]([C:15]#[N:16])[C:13]#[N:14])[N:3]=[CH:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
The product of stage (a) (26 g), aqueous dimethylamine (6.6 g) and ethanol (250 ml) were heated under reflux for 4 hours and then cooled to 0° C. Benzaldehyde N-methyl-N-[2,2-dicyano-1-(dimethylamino)ethenyl]hydrazone (19.8 g) precipitated, m.p. 127°-128° C.
Workup
- temperatureunder reflux for 4 hours
- customBenzaldehyde N-methyl-N-[2,2-dicyano-1-(dimethylamino)ethenyl]hydrazone (19.8 g) precipitated
Sources & evidence
- ORD record
- ord-4a1ea7f3ad294ec8898ecc90bef495cb
- Source dataset
- uspto-grants-1979_08
- Patent number
- US04163846
Reaction notes
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