Reaktionsgleichung
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Br:8])[C:3]=1[OH:9].CCO[C:13]([S-])=[S:14].[K+]>CCO>[Br:8][C:4]1[C:3]2[O:9][C:13]([SH:14])=[N:1][C:2]=2[CH:7]=[CH:6][CH:5]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
5 g (26.6 mmol) 2-amino-6-bromo-phenol are dissolved in 20 ml EtOH and 6.52 g (39.9 mmol) potassium ethyl xanthogenate are added. This mixture is stirred for 6 h at reflux temperature. After cooling to room temperature, the reaction mixture is concentrated in vacuo and 50 ml water are added. With the addition of acetic acid, a pH of 5 is adjusted. The product starts to crystallize and is filtered off, washed 2× with water and dried to afford the title compound.
Aufarbeitung
- temperatureat reflux temperature
- concentrationthe reaction mixture is concentrated in vacuo and 50 ml water
- additionare added
- additionWith the addition of acetic acid
- customto crystallize
- filtrationis filtered off
- washwashed 2× with water
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-663e6cbbc2c24d0084ee0ef8d1a887a7
- Quelldatensatz
- uspto-grants-2014_01
- Patentnummer
- US08629168B2
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