Calcium Acetate → Acrylamide

HRID 750430

Reaktionsgleichung

Reaktionsgleichung von HRID 750430
C([O-])(=[O:3])C.[Ca+2].C([O-])(=[O:8])C.[C:10](#[N:13])[CH:11]=[CH2:12].[C:14](#[N:18])[C:15]([CH3:17])=[CH2:16].[OH:19][CH:20]([CH2:24][CH3:25])[CH2:21][C:22]#[N:23]>O>[C:10]([NH2:13])(=[O:3])[CH:11]=[CH2:12].[C:14]([NH2:18])(=[O:8])[C:15]([CH3:17])=[CH2:16].[OH:19][CH:20]([CH2:24][CH3:25])[CH2:21][C:22]([NH2:23])=[O:3]

Komponenten

8

Edukt 4

HCID 6116Calcium AcetateHCID 7855AcrylonitrileHCID 31368MethacrylonitrileHCID 98554543-hydroxypentanenitrile

Produkt 3

HCID 6579AcrylamideHCID 6595MethacrylamideHCID 149797283-Hydroxypentanamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

At the completion of the reaction (100% conversion of nitrile), the product mixture was decanted from the biocatalyst beads, and additional distilled, deionized water, 0.2 mL of 0.20 M calcium acetate buffer (pH 7.0, 2.0 mM final calcium ion concentration in reaction mixture) and 10, 20, 40 or 60 mmol of acrylonitrile, methacrylonitrile, or 3-hydroxy-valeronitrile mixed with the reaction heel (immobilized-cell catalyst and remaining product mixture from the first reaction) at 25° C. or 35° C. At the completion of the second reaction, the product mixture was decanted and a third reaction performed as before. The reaction time, product yield for acrylamide, methacrylamide, or 3-hydroxyvaleramide, and the percent recovered biocatalyst activity for each recycle reaction is listed in Table 11 below.

Aufarbeitung

  1. customthe product mixture was decanted from the biocatalyst beads, and additional distilled
  2. additionmixed with the reaction heel (immobilized-cell catalyst
  3. customfrom the first reaction) at 25° C.
  4. custom35° C
  5. customAt the completion of the second reaction
  6. customthe product mixture was decanted
  7. customa third reaction

Quellen und Nachweise

ORD-Eintrag
ord-4d1d394c094b4ffdabf4d26c1dfe7bf0
Quelldatensatz
uspto-grants-2008_07
Patentnummer
US07405064B2

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