Hydrochloric Acid → 1,2,4-Thiadiazole-3-carboxylic acid, 5-chloro-, methyl ester
Reaktionsgleichung
N[C:2]1[S:6][N:5]=[C:4]([C:7]([O:9][CH3:10])=[O:8])[N:3]=1.[ClH:11].N([O-])=O.[Na+]>O.[Cu]>[Cl:11][C:2]1[S:6][N:5]=[C:4]([C:7]([O:9][CH3:10])=[O:8])[N:3]=1Komponenten
6
Reaktionsbedingungen
- Temperatur
- 50 °C
Versuchsvorschrift
To a mixture of methyl 5-amino-1,2,4-thiadiazole-3-carboxylate (26 g), conc.hydrochloric acid (490 ml) and a small amount of copper was added dropwise over 40 minutes a solution of sodium nitrite (22.5 g) in water (28 ml) at -10° to -15° C. The mixture was stirred for 1.5 hours at the same temperature and for 30 minutes at 50° C. The reaction mixture was poured into ice-water (500 ml) and extracted with ethyl acetate. The extract was washed, dried and concentrated to give white powder of methyl 5-chloro-1,2,4-thiadiazole-3-carboxylate (8.9 g).
Aufarbeitung
- extractionextracted with ethyl acetate
- washThe extract was washed
- customdried
- concentrationconcentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-620850f1f324403f981c8e85a9a62923
- Quelldatensatz
- uspto-grants-1984_05
- Patentnummer
- US04447429
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