m-Chloroperbenzoic acid → HCID 54571548, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([C:7]([O:9][CH:10]2[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]2)=[O:8])=[CH:3][C:2]=1[C:16]([O:18][CH:19]1[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]1)=[O:17].C1C=C(Cl)C=C(C(OO)=[O:33])C=1>>[N+:1]1([O-:33])[C:2]([C:16]([O:18][CH:19]2[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]2)=[O:17])=[CH:3][C:4]([C:7]([O:9][CH:10]2[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15]2)=[O:8])=[CH:5][CH:6]=1Participants
3
Procedure
From 1 g of dicyclohexyl pyridine-2,4-dicarboxylate and 0.75 g of MCPBA.
Sources & evidence
- ORD record
- ord-6795d0d7bb2240d6965ede52b81ce179
- Source dataset
- uspto-grants-1993_11
- Patent number
- US05260323
Reaction notes
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