Reaktionsgleichung
[CH3:1][NH:2][NH2:3].[CH3:4][O:5][C:6](=[O:12])/[CH:7]=[CH:8]\[C:9]([OH:11])=[O:10].[CH2:13]([N:15]([CH2:18][CH3:19])[CH2:16][CH3:17])[CH3:14].[CH:20](=O)[CH3:21]>C1COCC1>[CH2:13]([N:15]([CH2:18][CH3:19])[CH2:16][CH3:17])[CH3:14].[C:9]([CH:8]([N:2]([CH3:1])[N:3]=[CH:20][CH3:21])[CH2:7][C:6]([O:5][CH3:4])=[O:12])([OH:11])=[O:10]Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 88.5 g methylhydrazine (1.92 moles) in 340 ml THF is added at +25° C. to a solution of 250 g maleic acid monomethyl ester (1.92 moles) and 194.5 g triethylamine (1.92 moles) in 1850 ml THF. During the addition a precipitation of the triethylamine salt of the intermediate methyl 3-carboxy-3-(1-methyl-hydrazino)-propionate is formed. After stirring for 2 hours at +25° C., a solution of 101.6 g acetaldehyde (2.3 moles) in 370 ml THF is added at +25° C. The precipitation dissolves during the addition. After stirring for 1 hour at +25° C. the solution is evaporated completely. To remove traces of water or methanol, the residue is mixed with 750 ml toluene and evaporated again completely (10 mbar, 60° C.). Yield: 429.6 g of methyl 3-carboxy-3-(2-ethylidene-1-methylhydrazine)-propionate triethylamine salt as viscous yellow oil (83%).
Aufarbeitung
- additionDuring the addition
- customa precipitation of the triethylamine salt of the intermediate methyl 3-carboxy-3-(1-methyl-hydrazino)-propionate
- customis formed
- customThe precipitation
- dissolutiondissolves during the addition
- stirringAfter stirring for 1 hour at +25° C. the solution
- customis evaporated completely
- customTo remove traces of water or methanol
- additionthe residue is mixed with 750 ml toluene
- customevaporated again completely (10 mbar, 60° C.)
Quellen und Nachweise
- ORD-Eintrag
- ord-279630d299214a238c1364dceb47b59d
- Quelldatensatz
- uspto-grants-1997_09
- Patentnummer
- US05670648
Verknüpfte Notizen
Wird geladen…