Reaktionsgleichung
[N+:1]([CH2:4][C:5]([O:7]C)=[O:6])([O-:3])=[O:2].[CH3:9][N:10]1[CH2:14][CH2:13][N:12]=[C:11]1SC>C(O)(C)C>[CH3:9][N:10]1[CH2:14][CH2:13][NH:12][C:11]1=[C:4]([N+:1]([O-:3])=[O:2])[C:5]([OH:7])=[O:6]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
35.7 g methyl nitroacetate was added slowly to a refluxing mixture of 39.0 g of 1A and 300 ml of isopropyl alcohol. The mixture then was refluxed for 1 hour with provision to remove the methyl mercaptan by-product. The mixture was cooled and filtered to give the methyl ester of (1-methyl-2-imidazolidinylidene)nitroacetic acid (1B) as a solid, m.p.: 214°-217° (with decomposition).
Aufarbeitung
- temperatureThe mixture then was refluxed for 1 hour with provision
- customto remove the methyl mercaptan by-product
- temperatureThe mixture was cooled
- filtrationfiltered
Quellen und Nachweise
- ORD-Eintrag
- ord-e80e326091fc446892471a59408ec401
- Quelldatensatz
- uspto-grants-1977_10
- Patentnummer
- US04053619
Verknüpfte Notizen
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