Hydrochloric Acid → HCID 178467331, Verbindung
Reaktionsgleichung
C(O[C:4](=[O:16])[C:5](=[C:9]1[C:13](=[O:14])[NH:12][C:11](=[O:15])[NH:10]1)[O:6][CH2:7][CH3:8])C.[OH-:17].[K+].Cl>>[CH2:7]([O:6][C:5]1[C:9]([C:13]([OH:17])=[O:14])=[N:10][C:11]([OH:15])=[N:12][C:4]=1[OH:16])[CH3:8]Komponenten
4
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
(2,5-dioxo-imidazolidin-4-ylidene)-ethoxy-acetic acid ethyl ester (16.02 g, 1 eq.) was dissolved in aq. 1 N KOH (281 ml, 4 eq.) and refluxed for 3.5 hrs. The mixture was cooled to 0° C. and carefully acidified with conc. HCl. After overnight cooling (4° C.), it led to the formation of white precipitate. The mixture was filtered and the precipitate was dried in vacuo. The product obtained was a white solid (7.76 g, 55%).
Aufarbeitung
- temperaturerefluxed for 3.5 hrs
- temperatureAfter overnight cooling (4° C.), it
- filtrationThe mixture was filtered
- customthe precipitate was dried in vacuo
- customThe product obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-cfbb445fc17b4100b664f334c145addd
- Quelldatensatz
- uspto-grants-2016_04
- Patentnummer
- US09315491B2
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