Potassium Cation → 2,6-Bis(1-methylethyl)-4-phenoxybenzenamine

HRID 670778Notes

Reaction equation

HRID 670778 reaction equation
[Br:16][c:17]1[cH:18][c:19]([CH:27]([CH3:28])[CH3:29])[c:20]([NH2:21])[c:22]([CH:24]([CH3:25])[CH3:26])[cH:23]1.[C:1](=[O:2])([O-:3])[O-:4].[C:37](=[O:38])([O-:39])[O-:40].[CH3:30][c:31]1[cH:32][cH:33][cH:34][cH:35][cH:36]1.[Cu+2:41].[K+:15].[K+:5].[K+:6].[OH-:14].[OH2:42].[OH:7][c:8]1[cH:9][cH:10][cH:11][cH:12][cH:13]1>>[O:7]([c:8]1[cH:9][cH:10][cH:11][cH:12][cH:13]1)[c:17]1[cH:18][c:19]([CH:27]([CH3:28])[CH3:29])[c:20]([NH2:21])[c:22]([CH:24]([CH3:25])[CH3:26])[cH:23]1

Participants

9

Reactant 8

HCID 813Potassium Cation3×HCID 961HydroxideHCID 962WaterHCID 996PhenolHCID 1140TolueneHCID 19660Carbonate Ion2×HCID 27099Cupric cationHCID 117801144-Bromo-2,6-diisopropylaniline

Product 1

HCID 132721392,6-Bis(1-methylethyl)-4-phenoxybenzenamine

Sources & evidence

ORD record
ord-5cce11c0010a4e0bafca5fd1aa144f19
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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