Reaktionsgleichung
[CH3:1][O:2][C:3]([C:5]1[S:6][CH:7]=[CH:8][C:9]=1[OH:10])=[O:4].[C:11]([O-])([O-])=O.[K+].[K+].CI>CC(C)=O>[CH3:11][O:10][C:9]1[CH:8]=[CH:7][S:6][C:5]=1[C:3]([O:2][CH3:1])=[O:4]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 55 °C
Versuchsvorschrift
To a mixture of 3-hydroxy-thiophene-2-carboxylic acid methyl ester (5 g, 31.6 mmol) and K2CO3 (22.2 g, 161 mmol) in acetone (50 mL) is added CH3I (10.8 mL, 173 mmol,) dropwise at 0° C. The reaction mixture is heated at 55° C. for 4 hours, cooled to room temperature, filtered through diatomaceous earth, and the filtrate is concentrated under vacuum. The residue is diluted with water (100 mL) and extracted with ethyl acetate (2×200 mL). The combined organic layer is washed with brine solution (50 mL), dried over Na2SO4, and evaporated under vacuum to give title compound as a brown solid (5.9 g). ESI/MS m/z 173.1 (M+H)+.
Aufarbeitung
- temperaturecooled to room temperature
- filtrationfiltered through diatomaceous earth
- concentrationthe filtrate is concentrated under vacuum
- additionThe residue is diluted with water (100 mL)
- extractionextracted with ethyl acetate (2×200 mL)
- washThe combined organic layer is washed with brine solution (50 mL)
- dry with materialdried over Na2SO4
- customevaporated under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-b8852b3166384c15bf731c0a3791c52e
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08822486B2
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