Methyl Ethyl Ketone → 2,3-Dimethyl-4-(2,2,3,3,3-pentafluoropropoxy)pyridine-1-oxide
Reaction equation
[CH3:1][C:2]1[C:7]([CH3:8])=[C:6]([N+]([O-])=O)[CH:5]=[CH:4][N+:3]=1[O-:12].C(C(C)=O)C.[F:18][C:19]([F:26])([C:22]([F:25])([F:24])[F:23])[CH2:20][OH:21].C(=O)([O-])[O-].[K+].[K+]>CN(C)P(=O)(N(C)C)N(C)C>[CH3:1][C:2]1[C:7]([CH3:8])=[C:6]([O:21][CH2:20][C:19]([F:26])([F:18])[C:22]([F:25])([F:24])[F:23])[CH:5]=[CH:4][N+:3]=1[O-:12]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 2,3-dimethyl-4-nitropyridine-1-oxide (2.0 g), methyl ethyl ketone (30 ml), 2,2,3,3,3-pentafluoropropanol (3.05 ml), anhydrous potassium carbonate (3.29 g) and hexamethyl phosphoric acid triamide (2.07 g) was heated at 70°-80° C. for 4.5 days under stirring, then insolubles were filtered off. The filtrate was concentrated, to which was added water. The mixture was subjected to extraction with ethyl acetate. The extract solution was dried on magnesium sulfate, followed by removing the solvent by evaporation. The residue was chromatographed on a column of silica gel (50 g), eluted with chloroform-methanol (10:1), and recrystallized from ethyl acetate-hexane to yield 2.4 g of 2,3-dimethyl-4-(2,2,3,3,3-pentafluoropropoxy)pyridine-1-oxide as colorless needles, m.p. 148°-149° C.
Workup
- temperaturewas heated at 70°-80° C. for 4.5 days
- filtrationinsolubles were filtered off
- concentrationThe filtrate was concentrated, to which
- additionwas added water
- extractionThe mixture was subjected to extraction with ethyl acetate
- customThe extract solution was dried on magnesium sulfate
- customby removing the solvent
- customby evaporation
- customThe residue was chromatographed on a column of silica gel (50 g)
- washeluted with chloroform-methanol (10:1)
- customrecrystallized from ethyl acetate-hexane
Sources & evidence
- ORD record
- ord-e4ff6077d17347fd9c757525513074bb
- Source dataset
- uspto-grants-1987_08
- Patent number
- US04689333
Reaction notes
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