m-Chloroperbenzoic acid → HCID 178441440, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[NH:11][C:10]([CH2:12][CH2:13][CH2:14][CH3:15])=[N:9][C:5]2=[N:6][C:7]=1[CH3:8].ClC1C=CC=C(C(OO)=[O:24])C=1>C(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]2[NH:11][C:10]([CH2:12][CH2:13][CH2:14][CH3:15])=[N:9][C:5]2=[N+:6]([O-:24])[C:7]=1[CH3:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
7.8 g (29.1 mmole) of the compound obtained in step 4 was dissolved in 50 ml of methylene chloride and to the resulting solution was added 8.8 g (43.6 mmole) of 85% m-chloroperbenzoic acid. The resultant was stirred for 16 hours at room temperature and filtered to get a solid, which was washed with ethyl ether (12 ml×3) to obtain 8.0 g of the title compound (yield 97%).
Workup
- filtrationfiltered
- customto get a solid, which
- washwas washed with ethyl ether (12 ml×3)
Sources & evidence
- ORD record
- ord-534eb6e4a39140019444dbf493b98cfd
- Source dataset
- uspto-grants-1997_11
- Patent number
- US05691348
Reaction notes
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