2-Chloro-N,N-dimethyl-5-nitrobenzene-1-sulfonamide → 5-amino-2-chloro-N,N-dimethylbenzene-1-sulfonamide
Reaktionsgleichung
[CH3:1][N:2]([CH3:16])[S:3]([C:6]1[CH:11]=[C:10]([N+:12]([O-])=O)[CH:9]=[CH:8][C:7]=1[Cl:15])(=[O:5])=[O:4]>Cl>[CH3:1][N:2]([CH3:16])[S:3]([C:6]1[CH:11]=[C:10]([NH2:12])[CH:9]=[CH:8][C:7]=1[Cl:15])(=[O:5])=[O:4]Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 10 °C
Versuchsvorschrift
A mixture of 200 g of stannous chloride dihydrate and 250 ml of concentrated hydrochloric acid was cooled to 10° C. To the stirred mixture was added 50 g of N,N-dimethyl-2-chloro-5-nitrobenzenesulfonamide (Example A-2 above) in portions maintaining the temperature of 10° C. After removing the cooling bath, the reaction temperature rose to 55° C. and was held for two hours. The reaction mixture was cooled and filtered to remove the complex of the product with stannic chloride. The product was treated with water to decompose the complex and extracted with methylene chloride. Removal of solvent from the dried extract on a rotary evaporator gave 22 g of the title compound as a solid with a melting point of 125°-126° C.
Aufarbeitung
- temperaturemaintaining the temperature of 10° C
- customAfter removing the cooling bath
- customrose to 55° C.
- temperatureThe reaction mixture was cooled
- filtrationfiltered
- customto remove the complex of the product with stannic chloride
- additionThe product was treated with water
- extractionextracted with methylene chloride
- customRemoval of solvent from the dried
- extractionextract on a rotary evaporator
Quellen und Nachweise
- ORD-Eintrag
- ord-100c7d3b3f4642488a96e849ffdda7fd
- Quelldatensatz
- uspto-grants-1994_06
- Patentnummer
- US05324854
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