Reaktionsgleichung
[C:1]([O:11][CH2:12][CH3:13])(=[O:10])[CH:2]([CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6])[OH:3].Cl.[CH:15]([O:17][CH2:18][CH3:19])=[CH2:16]>>[CH2:15]([O:17][CH:18]([O:3][CH:2]([CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6])[C:1]([O:11][CH2:12][CH3:13])=[O:10])[CH3:19])[CH3:16]Komponenten
4
Versuchsvorschrift
A mixture of 19 g. diethyl malate and 0.1 g. of 36% hydrochloric acid was added to a 50 ml. round-bottom flask equipped with an addition funnel, static nitrogen head, condensor, heating mantle, thermometer, and magnetic stirrer. Ethyl vinyl ether was then added, dropwise, at 41° to 43° C. over a one-hour period and quenched with 0.4 g. of solid sodium carbonate. Distillation was performed directly on the mixture (short path column):
Aufarbeitung
- additionA mixture of 19 g
- customround-bottom flask equipped with an addition funnel
- temperaturestatic nitrogen head, condensor, heating mantle
- waitdropwise, at 41° to 43° C. over a one-hour period
- customquenched with 0.4 g
- distillationDistillation
Quellen und Nachweise
- ORD-Eintrag
- ord-03a0d5d11dcb4ebe840566a809e39380
- Quelldatensatz
- uspto-grants-1981_07
- Patentnummer
- US04280011
Verknüpfte Notizen
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