Reaktionsgleichung
NC1[S:3][C:4]2[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:5]=2[N:6]=1.[OH-].[K+].Cl>O>[NH2:6][C:5]1[CH:7]=[CH:8][C:9]([O:11][CH3:12])=[CH:10][C:4]=1[SH:3]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
34.3 g (0.19 mol) of 2-amino-6-methoxy-benzothiazole and 140 g (2.5 mol) of 85% potassium hydroxide are refluxed in 350 ml of water for 5 hours. Then the mixture is cooled and neutralised with 200 ml of concentrated hydrochloric acid. The mixture is stirred for a further 30 minutes, the precipitate formed is suction filtered, washed with water and dried in vacuo. Yield: 24.0 g (81.4% of theory). The following is obtained analogously to Example B:
Aufarbeitung
- temperatureThen the mixture is cooled
- customthe precipitate formed
- filtrationfiltered
- washwashed with water
- customdried in vacuo
- customThe following is obtained analogously to Example B
Quellen und Nachweise
- ORD-Eintrag
- ord-1b43938fb5074402905e3d3e73f51a4f
- Quelldatensatz
- uspto-grants-1999_07
- Patentnummer
- US05919807
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