Morpholine → 4-(4-Benzyloxy-3-nitro-phenyl)-morpholine

HRID 1060304Notes

Reaction equation

HRID 1060304 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]=1

Participants

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-1e8bfe610e6c4f85aa26bbd8c3b71dc6
Source dataset
uspto-grants-2003_02
Patent number
US06521754B2

Reaction notes

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