4-(p-Tolyloxy)aniline → HCID 86761608, compound
Reaction equation
[CH3:1]C1C=CC(OC2C=CC(N)=CC=2)=CC=1.[CH2:16]([N:20]([CH2:34][CH:35]1[O:37][CH2:36]1)[C:21]1[CH:26]=[CH:25][C:24]([O:27][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)=[CH:23][CH:22]=1)[CH:17]1[O:19][CH2:18]1>>[CH2:34]([N:20]([CH2:16][CH:17]1[O:19][CH2:18]1)[C:21]1[CH:22]=[CH:23][C:24]([O:27][C:28]2[CH:33]=[CH:32][C:31]([CH3:1])=[CH:30][CH:29]=2)=[CH:25][CH:26]=1)[CH:35]1[O:37][CH2:36]1Participants
3
Procedure
Except that 4-(4-methyl phenoxy)aniline was used as the amine compound acting as precursor for synthesizing the epoxy resin, the same procedures as for the N,N-diglycidyl-4-phenoxy aniline was carried out under the same reaction conditions for glycidyl formation, producing N,N-diglycidyl-4-(4-methyl phenoxy)aniline
Sources & evidence
- ORD record
- ord-29c924210ec94ca893b1d9418a3adc93
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08263216B2
Reaction notes
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