Benzyl Bromide → N-{4-[3-(allyloxy)phenoxy]benzyl}-N-benzyl-N-(2-methyl-3-nitrophenyl)amine

HRID 1370833Notes

Reaction equation

HRID 1370833 reaction equation
[CH2:1]([O:4][C:5]1[CH:6]=[C:7]([CH:27]=[CH:28][CH:29]=1)[O:8][C:9]1[CH:26]=[CH:25][C:12]([CH2:13][NH:14][C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([N+:21]([O-:23])=[O:22])[C:16]=2[CH3:24])=[CH:11][CH:10]=1)[CH:2]=[CH2:3].[CH2:30](Br)[C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1>>[CH2:1]([O:4][C:5]1[CH:6]=[C:7]([CH:27]=[CH:28][CH:29]=1)[O:8][C:9]1[CH:10]=[CH:11][C:12]([CH2:13][N:14]([CH2:30][C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([N+:21]([O-:23])=[O:22])[C:16]=2[CH3:24])=[CH:25][CH:26]=1)[CH:2]=[CH2:3]

Participants

3

Reactant 2

HCID 7498Benzyl BromideHCID 18512125N-(4-(3-(allyloxy)phenoxy)benzyl)-2-methyl-3-nitroaniline

Product 1

HCID 18512352N-{4-[3-(allyloxy)phenoxy]benzyl}-N-benzyl-N-(2-methyl-3-nitrophenyl)amine

Procedure

The product from Example 61D and benzyl bromide were processed as described in Example 6B to provide the title compound

Sources & evidence

ORD record
ord-ec703987e44b4244ab2b6b46d80e71ea
Source dataset
uspto-grants-2003_06
Patent number
US06583180B2

Reaction notes

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