m-Chloroperbenzoic acid → HCID 178526242, compound
Reaction equation
[F:1][C:2]([F:13])([F:12])[C:3]1[C:11]2[C:6](=[N:7][CH:8]=[CH:9][CH:10]=2)[NH:5][N:4]=1.ClC1C=C(C=CC=1)C(OO)=[O:19]>COCCOC.CCCCCCC>[F:13][C:2]([F:1])([F:12])[C:3]1[C:11]2[C:6](=[N+:7]([O-:19])[CH:8]=[CH:9][CH:10]=2)[NH:5][N:4]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Compound (1a) was dissolved in ethylene glycol dimethyl ether (100 mL) and heptane (200 mL), and m-chloroperoxybenzoic acid (33.9 g) was added to the resulting solution at 0° C., followed by stirring at room temperature for 1 hr. The precipitate was collected by filtration to obtain compound (1b) (33.3 g, 96%) as a white solid.
Workup
- filtrationThe precipitate was collected by filtration
Sources & evidence
- ORD record
- ord-037d1885348b42d3b15871185524f3d0
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08779142B2
Reaction notes
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