Morpholine → 4-(4-Benzyloxy-3-nitro-phenyl)-morpholine
Reaction equation
[NH:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[CH2:7]([O:14][C:15]1[CH:20]=[CH:19][C:18](Br)=[CH:17][C:16]=1[N+:22]([O-:24])=[O:23])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.COC1C=CC(N2CCOCC2)=CC=1[N+]([O-])=O>>[CH2:7]([O:14][C:15]1[CH:20]=[CH:19][C:18]([N:1]2[CH2:6][CH2:5][O:4][CH2:3][CH2:2]2)=[CH:17][C:16]=1[N+:22]([O-:24])=[O:23])[C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1Participants
4
Procedure
The title compound was prepared using morpholine and 1-benzyloxy-4-bromo-2-nitro-benzene (prepared from 4-bromo-2-nitro-anisol and benzyl bromide) using the general method of example “4-(4-methoxy-3-nitro-phenyl)-morpholine” as yellow solid (58%), MS: m/e=315(M+H+).
Sources & evidence
- ORD record
- ord-055d163dad4844af8496feba2f4cc17b
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06835732B2
Reaction notes
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