4-Chloro-2-(2,4-dinitroanilino)phenol → 2-(2-Nitroanilino)phenol
Reaction equation
Cl[C:2]1[CH:3]=[CH:4][C:5]([OH:21])=[C:6]([NH:8][C:9]2[CH:14]=[CH:13][C:12]([N+]([O-])=O)=[CH:11][C:10]=2[N+:18]([O-:20])=[O:19])[CH:7]=1.[N+](C1C=C([N+]([O-])=O)C=CC=1N1C2C=C(Cl)C=CC=2OC1=O)([O-])=O>>[OH:21][C:5]1[CH:4]=[CH:3][CH:2]=[CH:7][C:6]=1[NH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[N+:18]([O-:20])=[O:19]Participants
3
Procedure
N-(5-chloro-2-hydroxyphenyl)-2,4-dinitroaniline from N-(2,4-dinitrophenyl)-5-chloro-2-benzoxazolinone. The product was used without further purification.
Workup
- customThe product was used without further purification
Sources & evidence
- ORD record
- ord-c3ee6d19a4444ac9b43db64553b2d774
- Source dataset
- uspto-grants-1993_04
- Patent number
- US05200422
Reaction notes
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