2-Methoxy-4-nitroaniline → HCID 20565335, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1[CH:19]=[CH:18][C:5]([C:6](NC2C=CC(N)=CC=2OC)=[O:7])=[CH:4][CH:3]=1.COC1C=C([N+]([O-])=O)C=CC=1N.[Cl:32][C:33]1[CH:39]=[C:38]([N+:40]([O-])=O)[CH:37]=[C:36]([Cl:43])[C:34]=1[NH2:35]>>[NH2:1][C:2]1[CH:19]=[CH:18][C:5]([C:6]([NH:35][C:34]2[C:33]([Cl:32])=[CH:39][C:38]([NH2:40])=[CH:37][C:36]=2[Cl:43])=[O:7])=[CH:4][CH:3]=1Komponenten
4
Versuchsvorschrift
By operating as described under (a) above, but using instead of 202 parts of 2-methoxy-4-nitro-aniline, 248 parts of 2,6-dichloro-4-nitro-aniline, high yields of 4,4'-diamino-2'6'-dichloro-benzanilide were obtained.
Quellen und Nachweise
- ORD-Eintrag
- ord-35d28761a76b4704ad62ee81aae07672
- Quelldatensatz
- uspto-grants-1981_05
- Patentnummer
- US04269769
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