Sodium Dithionite → 2-(4-Aminophenylamino)ethanesulfonamide
Reaktionsgleichung
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:10][CH2:11][CH2:12][S:13]([NH2:16])(=[O:15])=[O:14])=[CH:6][CH:5]=1)([O-])=O.S(S([O-])=O)([O-])=O.[Na+].[Na+]>C(O)C>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([NH:10][CH2:11][CH2:12][S:13]([NH2:16])(=[O:14])=[O:15])=[CH:8][CH:9]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
1 g of 2-(4-nitrophenylamino)ethanesulfonamide (12) was suspended in 10 mL of ethanol. At room temperature, the suspension was poured onto a reductive solution of sodium hydrosulfite (8 g)—1N sodium hydroxide (30 mL). After decolorization, a precipitate formed. 0.7 g of crude product was isolated by suction-filtering and reslurrying in water.
Aufarbeitung
- customAfter decolorization, a precipitate formed
Quellen und Nachweise
- ORD-Eintrag
- ord-2535bde458e24411a61dd72c00e52b04
- Quelldatensatz
- uspto-grants-2008_03
- Patentnummer
- US07347879B2
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