Pyridine →
Reaction equation
[Cl:1][CH2:2][C:3](=[O:10])[CH2:4][C:5]([O:7]CC)=[O:6].[N:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>>[Cl-:1].[C:5]([O-:7])(=[O:6])[CH2:4][C:3]([CH3:2])=[O:10].[CH2:2]([C:12]1[CH:13]=[CH2+:14][CH:15]=[CH:16][N:11]=1)[CH3:3].[CH2:2]([C:12]1[CH:13]=[CH2+:14][CH:15]=[CH:16][N:11]=1)[CH3:3]Participants
2
Reactant 2
Product 0
No Product data yet.
Procedure
The title compound was prepared as described in Example 1 from pyridine and ethyl 4-chloroacetoacetate in a yield of 70%.
Sources & evidence
- ORD record
- ord-a523251841d246209abff968cf749a1e
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05438140
Reaction notes
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