N-Phenyl-p-phenylenediamine → 195133-09-6
Reaction equation
[C:1]1([NH:7][C:8]2[CH:13]=[CH:12][C:11]([NH2:14])=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:15]1(=[O:21])[O:20][C:18](=[O:19])[CH2:17][CH2:16]1>>[NH:7]([C:8]1[CH:13]=[CH:12][C:11]([NH:14][C:15](=[O:21])[CH2:16][CH2:17][C:18]([OH:20])=[O:19])=[CH:10][CH:9]=1)[C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
3
Procedure
The experimental protocol used is the same as that described in J. Amer. Chem. Soc. (1951) 73, 4007, starting from N1-phenyl-1,4-benzenediamine and succinic anhydride in order to produce a pale grey-blue powder. Melting point: 175-176° C.
Workup
- customto produce a pale grey-blue powder
Sources & evidence
- ORD record
- ord-ff6e725ba9404601858d5401af3031ab
- Source dataset
- uspto-grants-2004_06
- Patent number
- US06747024B1
Reaction notes
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