Methacrylonitrile → HCID 13050978, compound
Reaction equation
[Na].[Cl:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([NH:9][NH2:10])[N:4]=1.[C:11](#[N:15])[C:12]([CH3:14])=[CH2:13]>C(O)C>[NH2:15][C:11]1[CH:12]([CH3:14])[CH2:13][N:9]([C:5]2[CH:6]=[CH:7][CH:8]=[C:3]([Cl:2])[N:4]=2)[N:10]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
As for Example 2 a 0.32 g. amount of sodium metal is dissolved in 100 ml. of absolute ethanol, then 10.0 g. of 2-chloro-6-hydrazinopyridine is added, followed by 4.8 g. of methacrylonitrile in place of acrylonitrile. The procedure of Example 2 is followed to give 9.4 g. of crude product. The material is recrystallized from dichloromethane-hexane to give the product of the Example as pale yellow crystals, m.p. 175°-176° C.
Workup
- customto give 9.4 g
- customThe material is recrystallized from dichloromethane-hexane
- customto give the product of the Example as pale yellow crystals, m.p. 175°-176° C.
Sources & evidence
- ORD record
- ord-b3bc17991c6f4a1e8138691b9d5cdb4f
- Source dataset
- uspto-grants-1986_11
- Patent number
- US04622401
Reaction notes
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