Pyridine → Ethyl 1-(2-acetoxyethyl)pyrrole-2-glyoxalate
Reaktionsgleichung
N1C=CC=CC=1.[C:7](Cl)([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[O:8].[C:15]([O:18][CH2:19][CH2:20][N:21]1[CH:25]=[CH:24][CH:23]=[CH:22]1)(=[O:17])[CH3:16]>ClCCl>[C:15]([O:18][CH2:19][CH2:20][N:21]1[CH:22]=[CH:23][CH:24]=[C:25]1[C:7](=[O:8])[C:9]([O:11][CH2:12][CH3:13])=[O:10])(=[O:17])[CH3:16]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In the next step, a solution of pyridine in anhydrous dichloromethane is added to a stirred and cooled solution of ethoxalyl chloride in anhydrous dichloromethane so that the reaction temperature remains at about -20° to -25° C. Upon completion of this addition an approximately equimolar amount of 1-(2-acetoxyethyl)pyrrole of Formula (III) in anhydrous dichloromethane is added while the temperature is maintained at temperatures of about 0° to -20° C. Washing with water, drying, removal of the solvent and purification gives ethyl 1-(2-acetoxyethyl)pyrrole-2-glyoxylate.
Aufarbeitung
- customremains at about -20° to -25° C
- additionis added while the temperature
- temperatureis maintained at temperatures of about 0° to -20° C
- washWashing with water
- customdrying
- customremoval of the solvent and purification
Quellen und Nachweise
- ORD-Eintrag
- ord-ec5a8ef743984bf294e6074f301440ea
- Quelldatensatz
- uspto-grants-1982_08
- Patentnummer
- US04344943
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