Hydrochloric Acid → 4-[(Pyridin-2-yl)sulfanyl]benzene-1,2-diamine
Reaktionsgleichung
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=2)=[CH:4][C:3]=1[N+:15]([O-])=O.Cl.C(=O)(O)[O-].[K+]>>[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=2)=[CH:4][C:3]=1[NH2:15]Komponenten
4
Versuchsvorschrift
2.3 G. of 1-amino-2-nitro-4-(pyrid-2-ylthio)benzene in 12 ml. concentrated hydrochloric acid is treated with 12 g. of stannous chloride on the steam bath for 15 minutes. The cooled solution is treated with an excess of potassium bicarbonate and extracted with chlorofrom and filtered. The chloroform layer is separated, dried and evaporated to yield 1,2-diamino-4-(pyrid-2-ylthio)benzene.
Aufarbeitung
- extractionextracted with chlorofrom
- filtrationfiltered
- customThe chloroform layer is separated
- customdried
- customevaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-682bb6378d9445ae913ff34afacdcf14
- Quelldatensatz
- uspto-grants-1976_01
- Patentnummer
- US03935209
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