Sodium Sulfite → 2-[(Z)-C-(3-bromophenyl)-N-[(2-methylpropan-2-yl)oxy]carbonimidoyl]-1-oxidopyridin-1-ium-3-ol
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:19]=[CH:20][CH:21]=1)/[C:5](/[C:12]1[C:17]([OH:18])=[CH:16][CH:15]=[CH:14][N:13]=1)=[N:6]/[O:7][C:8]([CH3:11])([CH3:10])[CH3:9].ClC1C=CC=C(C(OO)=[O:30])C=1.S([O-])([O-])=O.[Na+].[Na+]>O1CCCC1>[Br:1][C:2]1[CH:3]=[C:4]([CH:19]=[CH:20][CH:21]=1)/[C:5](/[C:12]1[C:17]([OH:18])=[CH:16][CH:15]=[CH:14][N+:13]=1[O-:30])=[N:6]/[O:7][C:8]([CH3:11])([CH3:9])[CH3:10]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of (Z)-2-(3-bromo-α-t-butoxyiminobenzyl)-3-hydroxypyridine (0.49 g), 70% m-chloroperbenzoic acid (0.70 g) and tetrahydrofuran (30 mL) was stirred overnight at room temperature. To the reaction mixture was added an aqueous solution of sodium sulfite. The reaction mixture was stirred for 30 minutes, and extracted with ethyl acetate. The extract was washed with water and a saturated aqueous saline solution, successively, and dried (sodium sulfate) and then concentrated. The concentrate was crystallized from isopropyl ether, and recrystallized from ethanol-water to afford (Z)-2-(3-bromo-α-t-butoxyiminobenzyl)-3-hydroxypyridine 1-oxide (0.41 g) (compound 3). In substantially the same manner as above, compounds 4, 7, 8, 11, 12 and 15 were produced.
Workup
- stirringThe reaction mixture was stirred for 30 minutes
- extractionextracted with ethyl acetate
- washThe extract was washed with water
- dry with materiala saturated aqueous saline solution, successively, and dried (sodium sulfate)
- concentrationconcentrated
- customThe concentrate was crystallized from isopropyl ether
- customrecrystallized from ethanol-water
Sources & evidence
- ORD record
- ord-78d0cdbe93ec4f1d9b058afdc5fef559
- Source dataset
- uspto-grants-1999_04
- Patent number
- US05891895
Reaction notes
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