Hydrazine → HCID 178441976, compound
Reaction equation
[NH2:1][NH2:2].Cl[C:4]([C:10]([CH3:13])([CH3:12])[CH3:11])=[C:5]([C:8]#[N:9])[C:6]#[N:7]>C(O)C>[NH2:7][C:6]1[NH:2][N:1]=[C:4]([C:10]([CH3:13])([CH3:12])[CH3:11])[C:5]=1[C:8]#[N:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Hydrazine (40 g) was dissolved in ethanol (100 ml) and was placed in a flask equipped with a condenser, a dropping funnel, a thermometer and a magnetic stirrer. A solution of the above pentenenitrile intermediate (b) (80 g) in ethanol (300 ml) was added with stirring at a rate that the temperature did not rise above 35° C. The reaction mixture was then gently refluxed for 90 minutes, the solvent was partially removed and the residue was treated with water. The product was filtered off and dried.
Workup
- customwas placed in a flask
- customequipped with a condenser, a dropping funnel
- customdid not rise above 35° C
- temperatureThe reaction mixture was then gently refluxed for 90 minutes
- customthe solvent was partially removed
- additionthe residue was treated with water
- filtrationThe product was filtered off
- customdried
Sources & evidence
- ORD record
- ord-8792ab13897544d3847a1ae5393a7c93
- Source dataset
- uspto-grants-1992_09
- Patent number
- US05144015
Reaction notes
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