Reaktionsgleichung
C[O:2][C:3]([C:5]1[CH:9]=[C:8]([C:10]2[N:11]=[CH:12][O:13][CH:14]=2)[S:7][CH:6]=1)=[O:4].[OH-].[Na+]>>[O:13]1[CH:14]=[C:10]([C:8]2[S:7][CH:6]=[C:5]([C:3]([OH:4])=[O:2])[CH:9]=2)[N:11]=[CH:12]1Komponenten
3
Versuchsvorschrift
5-Oxazol-4-yl-thiophene-3-carboxylic acid methyl ester (0.049 g, 0.23 mmol) was suspended in IMS (1 mL), sodium hydroxide (1 M, 0.35 mL) was added and the mixture stirred for 60 hours at room temperature. The mixture was quenched with HCl (1 N, 0.35 mL) and then concentrated, azeotroping twice with methanol to afford 5-oxazol-4-yl-thiophene-3-carboxylic acid as a white solid (0.045 g).
Aufarbeitung
- customThe mixture was quenched with HCl (1 N, 0.35 mL)
- concentrationconcentrated
- customazeotroping twice with methanol
Quellen und Nachweise
- ORD-Eintrag
- ord-a9e15b923af248999376c9b186edc511
- Quelldatensatz
- uspto-grants-2012_10
- Patentnummer
- US08299063B2
Verknüpfte Notizen
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