Hydrogen Peroxide → HCID 23003412, compound
Reaction equation
[CH2:1]([C:3]1[CH:8]=[CH:7][N:6]=[CH:5][C:4]=1[F:9])[CH3:2].[OH:10]O>C(O)(=O)C>[CH2:1]([C:3]1[CH:8]=[CH:7][N+:6]([O-:10])=[CH:5][C:4]=1[F:9])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a mixture of 4-ethyl-3-fluoropyridine (R. P. Dikinson et al., Bioorg. Med. Chem. Lett., 1996, 6, 2031, 28.51 g, 205.9 mmol) and 30% hydrogen peroxide (30 ml) in acetic acid (300 ml) was heated at reflux temperature for 3 h. After cooling to room temperature, the resulting mixture was concentrated. The residue was diluted in dichloromethane (300 ml) and dried (MgSO4). Removal of solvent gave 32.30 g (100%) of the title compound as an oil.
Workup
- temperaturewas heated
- temperatureat reflux temperature for 3 h
- concentrationthe resulting mixture was concentrated
- additionThe residue was diluted in dichloromethane (300 ml)
- dry with materialdried (MgSO4)
- customRemoval of solvent
Sources & evidence
- ORD record
- ord-a31482cfa84f41f79352520aacc30225
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06608070B1
Reaction notes
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