Reaktionsgleichung
[CH3:1][C:2](=[O:7])[CH2:3][CH2:4][CH2:5][CH3:6].[NH2-].[Na+].[CH3:10][O:11][CH2:12][C:13](OC)=[O:14].Cl>CCOCC>[CH3:10][O:11][CH2:12][C:13](=[O:14])[CH2:1][C:2](=[O:7])[CH2:3][CH2:4][CH2:5][CH3:6]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2-Hexanone (96.8 g) was added dropwise over 15 min under nitrogen to a stirred suspension of sodium amide (37.7 g) in dry ether (1 liter) at room temperature. The mixture was stirred for 12 min, a solution of methyl methoxyacetate (50.3 g) in dry ether (150 ml) was added dropwise over 20 min, and the mixture was heated under reflux for 2 h. The mixture was cooled, poured into ice and 2N hydrochloric acid (600 ml) and the aqueous layer extracted with ether (4×300 ml). The organic layers were washed with 8% sodium bicarbonate solution and brine, dried and evaporated to give an orange liquid (102 g). Purification by DFC, eluting with System A (5:95) gave a yellow liquid (36 g).
Aufarbeitung
- temperaturethe mixture was heated
- temperatureunder reflux for 2 h
- temperatureThe mixture was cooled
- extractionthe aqueous layer extracted with ether (4×300 ml)
- washThe organic layers were washed with 8% sodium bicarbonate solution and brine
- customdried
- customevaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-694a9480f5a84dfb9d79b562632804fb
- Quelldatensatz
- uspto-grants-1995_02
- Patentnummer
- US05389659
Verknüpfte Notizen
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