Reaktionsgleichung
[Br:1][C:2]1[C:3]([CH3:13])=[N:4][N:5]([CH3:12])[C:6]=1[C:7]([O:9]CC)=[O:8].[OH-].[Na+]>CO>[Br:1][C:2]1[C:3]([CH3:13])=[N:4][N:5]([CH3:12])[C:6]=1[C:7]([OH:9])=[O:8]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 20 °C
Versuchsvorschrift
To a solution of ethyl 4-bromo-1,3-dimethyl-1H-pyrazole-5-carboxylate (200 mg) (for example, available from Sinova) in methanol (10 ml) was added 2M sodium hydroxide (5 ml) and the mixture stirred at 20° C. for 18 h. The mixture was concentrated in vacuo and the residue taken up in water (10 ml) and acidified to pH=5 using 2M hydrochloric acid. The mixture was extracted with ethyl acetate (20 ml) dried over sodium sulphate and evaporated to give the title compound (25 mg) as a white solid.
Aufarbeitung
- concentrationThe mixture was concentrated in vacuo
- extractionThe mixture was extracted with ethyl acetate (20 ml)
- dry with materialdried over sodium sulphate
- customevaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-892f17811ad04ed5ba0471035bfa38ca
- Quelldatensatz
- uspto-grants-2014_02
- Patentnummer
- US08658635B2
Verknüpfte Notizen
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