Dimethylamine → Ethyl 2-cyano-3-(dimethylamino)acrylate
Reaktionsgleichung
[CH3:1][NH:2][CH3:3].[C:4]([CH2:6][C:7]([O:9][CH2:10][CH3:11])=[O:8])#[N:5].[OH-].[Na+].[C:14]1(C)C=CC=CC=1>>[CH3:1][N:2]([CH:14]=[C:6]([C:4]#[N:5])[C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH3:3]Komponenten
5
Reaktionsbedingungen
- Temperatur
- 20 °C
Versuchsvorschrift
5.5 g of dimethylamine were condensed with 20.9 g of methoxymethyleneiminium methylsulphate at 0° C. After stirring for 1 hour at 20° C., excess dimethylamine and 70% of the resulting methanol were removed in vacuo. Analogously to Example 1, the salt obtained was reacted with 11.4 g of ethyl cyanoacetate and 4.0 g of NaOH in 140 ml of toluene. 93% of ethyl dimethylaminomethylenecyano-acetate were obtained, together with 1.2% of the corresponding methyl ester.
Aufarbeitung
- customexcess dimethylamine and 70% of the resulting methanol were removed in vacuo
- customAnalogously to Example 1, the salt obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-ac039ce1701846b5b9325fee84f94c89
- Quelldatensatz
- uspto-grants-1993_08
- Patentnummer
- US05241099
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