m-Chloroperbenzoic acid → 5-Bromo-2-chloro-1-oxo-1lambda~5~-pyridine
Reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:8])=[N:6][CH:7]=1.ClC1C=CC=C(C(OO)=[O:17])C=1>C(Cl)(Cl)Cl.C(OCC)(=O)C.CCCCCC>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:8])=[N+:6]([O-:17])[CH:7]=1Participants
6
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Conditions
- Temperature
- 60 °C
Procedure
To a solution of 5-bromo-2-chloropyridine (1.0 eq.) in chloroform (0.38 M) was added 77% meta-chloroperbenzoic acid (mCPBA) (4.0 eq.) and heated at 60° C. for 20 hours. After cooling to room temperature, Ca(OH)2 (5.3 eq.) was added, and the resulting precipitate was stirred for 30 minutes. The precipitate was filtered and washed with 3:1 CHCl3/methanol. The filtrate was concentrated en vacuo to give a solid, which was stirred in 30% ethyl acetate in hexane and filtered to give the desired N-oxide. The filtrate was concentrated en vacuo, and the residue was purified by a COMBIFLASH® system (ISCO) using 0-100% ethyl acetate in hexane to give more of the desired N-oxide. The two batches were combined and carried onto the next step.
Workup
- temperatureAfter cooling to room temperature
- filtrationThe precipitate was filtered
- washwashed with 3:1 CHCl3/methanol
- concentrationThe filtrate was concentrated en vacuo
- customto give a solid, which
- filtrationfiltered
Sources & evidence
- ORD record
- ord-91eac63631534069b77e5e3fd7271f07
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08895577B2
Reaction notes
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