Hydrochloric Acid → 2-Chloro-1,3-thiazole-4-carboxylic acid
Reaktionsgleichung
N[C:2]1[S:3][CH:4]=[C:5]([C:7]([OH:9])=[O:8])[N:6]=1.[ClH:10].N([O-])=O.[Na+].O>O1CCOCC1.[Cu](Cl)Cl.C(OCC)(=O)C>[Cl:10][C:2]1[S:3][CH:4]=[C:5]([C:7]([OH:9])=[O:8])[N:6]=1Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
To a solution of 2.84 g (19.7 mmol) of 2-aminothiazole-4-carboxylic acid in 30 ml of 1,4-dioxane was added 50 ml of concentrated hydrochloric acid, followed by cooling to 0° C., and 10 ml of an aqueous solution of 2.04 g (29.6 mmol) of sodium nitrite was added charged dropwise thereto at 0° C. to 5° C. The reaction liquid was stirred at 0° C. for 2 hours, and then 2.93 g (29.6 mmol) of copper chloride was charged in separate portions thereto. The reaction liquid was returned to room temperature, followed by stirring for 8 hours. To the reaction liquid were added water and ethyl acetate, followed by extraction with ethyl acetate four times. The organic layer was washed with saturated brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to prepare 1.77 g (yield 55%) of a target compound.
Aufarbeitung
- additioncharged dropwise
- customat 0° C. to 5° C
- customThe reaction liquid
- customThe reaction liquid
- customwas returned to room temperature
- stirringby stirring for 8 hours
- customTo the reaction liquid
- extractionfollowed by extraction with ethyl acetate four times
- washThe organic layer was washed with saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- customThe solvent was evaporated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-e2ff88eb760a41e29dc6f9fa5d883660
- Quelldatensatz
- uspto-grants-2016_01
- Patentnummer
- US09237745B2
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