Reaktionsgleichung
[CH2:1]([O:3][C:4](=[O:13])[C:5]([CH3:12])([CH3:11])[C:6]([O:8]CC)=[O:7])[CH3:2].[OH-].[K+]>C(O)C>[CH2:1]([O:3][C:4](=[O:13])[C:5]([CH3:12])([CH3:11])[C:6]([OH:8])=[O:7])[CH3:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
25 g 2,2-Dimethyl-malonic acid diethyl ester, 7.8 g potassium hydroxide and 500 ml ethanol were mixed in a round-bottomed flask and refluxed for 3 hours. Then again 2.2 g potassium hydroxide were added and the mixture was refluxed overnight. The solvent was removed on a rotovap, 250 ml H2O were added and the mixture was washed with ether. The aqueous phase was acidified with HCl to pH 3-4 followed by two extractions with dichloromethane. The organic solvent was dried and evaporated and the resulting product was characterized by 1H-NMR.
Aufarbeitung
- temperaturerefluxed for 3 hours
- temperaturethe mixture was refluxed overnight
- customThe solvent was removed on a rotovap, 250 ml H2O
- additionwere added
- washthe mixture was washed with ether
- extractionfollowed by two extractions with dichloromethane
- customThe organic solvent was dried
- customevaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-d05ddce2c4654619837edad593ea50d2
- Quelldatensatz
- uspto-grants-2016_03
- Patentnummer
- US09283186B2
Verknüpfte Notizen
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