m-Chloroperbenzoic acid → 2-Bromo-3-fluoropyridine 1-oxide
Reaction equation
[Br:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[CH:4][N:3]=1.ClC1C=CC=C(C(OO)=[O:17])C=1>C(Cl)(Cl)Cl>[Br:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[CH:4][N+:3]=1[O-:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 50 °C
Procedure
A mixture of 2-bromo-3-fluoropyridine (1.0 g, 5.7 mmol) and 3-chloroperbenzoic acid (1.5 g, 7.4 mmol) in chloroform (3.5 mL) was stirred at 50° C. for 18 hours, cooled down to room temperature and filtered. The filtrate was concentrated under reduced pressure to give a residue that was purified by flash chromatography (Si—PPC, MeOH:EtOAc, gradient 0:100 to 5:95) to give 2-Bromo-3-fluoropyridine 1-oxide as a white solid (878 mg, 80%). 1H NMR (400 MHz, CHCl3-d): δ 8.25 (dt, J=6.6, 1.3 Hz, 1 H); 7.25-7.17 (m, 1 H); 7.06 (ddd, J=8.7, 6.6, 1.3 Hz, 1 H).
Workup
- temperaturecooled down to room temperature
- filtrationfiltered
- concentrationThe filtrate was concentrated under reduced pressure
- customto give a residue that
- customwas purified by flash chromatography (Si—PPC, MeOH:EtOAc, gradient 0:100 to 5:95)
Sources & evidence
- ORD record
- ord-0c6de4def1ca4255ab5ee059c780c285
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08394796B2
Reaction notes
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