Reaktionsgleichung
[NH:1]1[C:5](=[O:6])[CH2:4][CH2:3][C@H:2]1[C:7]([OH:9])=[O:8].CO.OS(O)(=O)=O.[C:17]([O-])(O)=O.[Na+]>C1COCC1>[CH3:17][O:8][C:7](=[O:9])[C@@H:2]1[CH2:3][CH2:4][C:5](=[O:6])[NH:1]1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 60 °C
Versuchsvorschrift
A 500 g sample of L-pyroglutamic acid was added to 2.8 L of anhydrous methanol, 28 mL of H2SO4 was added, and the mixture was stirred for 4 hr at 60° C. The reaction mixture was cooled to room temperature, 262 g of NaHCO3 was added, and the mixture was stirred for an additional 16 hr. The mixture was dried by addition of 314 g of Na2SO4 with stirring for 1 hr, then the mixture was filtered and the solvent was evaporated under vacuum to yield a pale yellow oil. The oil was dissolved in THF, and a small amount of unreacted acid was filtered off. The THF was removed under vacuum, and the residual oil was dried by azeotropic distillation with toluene.
Aufarbeitung
- additionwas added
- temperatureThe reaction mixture was cooled to room temperature
- stirringthe mixture was stirred for an additional 16 hr
- dry with materialThe mixture was dried by addition of 314 g of Na2SO4
- stirringwith stirring for 1 hr
- filtrationthe mixture was filtered
- customthe solvent was evaporated under vacuum
- customto yield a pale yellow oil
- filtrationa small amount of unreacted acid was filtered off
- customThe THF was removed under vacuum
- dry with materialthe residual oil was dried by azeotropic distillation with toluene
Quellen und Nachweise
- ORD-Eintrag
- ord-0c770679fe32403da5c7fc2799431ed7
- Quelldatensatz
- uspto-grants-1995_06
- Patentnummer
- US05424444
Verknüpfte Notizen
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