HCID 14598772, compound → HCID 18360905, compound
Reaction equation
[N+:1]([C:4]1([N+:10]([O-:12])=[O:11])[CH2:9][O:8]C(=O)[CH2:5]1)([O-:3])=[O:2].[N+](C(C)C(O)=O)([O-])=[O:14]>>[N+:1]([C:4]([N+:10]([O-:12])=[O:11])([CH3:5])[C:9]([OH:14])=[O:8])([O-:3])=[O:2]Participants
3
Procedure
A unique synthesis involving the latter substrates covers the synthesis of 3,3-dinitrobutyrolactone. 2-nitropropionic acid can be nitrated to provide 2,2-dinitropropionic acid, which is formylated to give the corresponding methylol derivative, which is then cyclized to the lactone.
Workup
- customA unique synthesis
Sources & evidence
- ORD record
- ord-17f86ade9544497f8983fcd88557d6ca
- Source dataset
- uspto-grants-1986_06
- Patent number
- US04594430
Reaction notes
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