Reaktionsgleichung
[OH:1][CH2:2][CH:3]([CH2:5][OH:6])[OH:4].[C:7](OCC)(=[O:12])[CH2:8][C:9]([CH3:11])=[O:10].C1C(CCCCC(N)=O)SSC1>C(O)C>[CH3:11][C:9]([CH2:8][C:7]([O:1][CH2:2][CH:3]([OH:4])[CH2:5][OH:6])=[O:12])=[O:10]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In accordance with at least one other embodiment of the present technology, glycerol can be treated with ethyl acetoacetate in presence of a lipase at from about 55° C. to about 70° C., alternatively from about 20 to about 75, for approximately 14 to 48 hours, alternatively 20 to 36 hours. The lipase can be, for example, Novozyme® 435, Lipozyme® RM IM, or Lipozyme® TL IM, all available from Novozymes A/S, Franklinton, N.C. The reaction can be performed in an inert (e.g., nitrogen) atmosphere. During the reaction, ethyl alcohol by-product can be removed, for example, via distillation. At the end of the reaction, the remaining ethyl acetoacetate can be removed through distillation (e.g., at 60° C., 1 mmHg). The structure of the triglyceride of acetoacetin produced can be confirmed through, for example, NMR analysis and/or GC.
Aufarbeitung
- customThe reaction
- customAt the end of the reaction
- customthe remaining ethyl acetoacetate can be removed through distillation (e.g., at 60° C., 1 mmHg)
Quellen und Nachweise
- ORD-Eintrag
- ord-51a29cc064194e87bb7a54163f2db38a
- Quelldatensatz
- uspto-grants-2010_10
- Patentnummer
- US07807718B2
Verknüpfte Notizen
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