Reaktionsgleichung
[C:1]([O:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH:11]([CH3:13])[CH3:12])(=[O:4])[CH:2]=[CH2:3].[CH:14]([N:16]1[CH2:20][CH2:19][CH2:18][C:17]1=[O:21])=[CH2:15].CCCCCCC>C(OCC)(=O)C>[C:1]([O:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH:11]([CH3:13])[CH3:12])(=[O:4])[CH:2]=[CH2:3].[CH:14]([N:16]1[CH2:20][CH2:19][CH2:18][C:17]1=[O:21])=[CH2:15]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 55 °C
Versuchsvorschrift
Isooctyl acrylate (54.9 Kg), N-vinyl-2-pyrrolidone (5.4 Kg), and ethyl acetate (93.6 Kg) were charged into a 75 gallon (285 liter) stainless steel reactor. The mixture was deoxygenated and heated to 55° C. After 5 minutes at 55° C., azobisisobutyronitrile (30 g) premixed in ethyl acetate (1 Kg) was charged to the reactor. Additional portions of azobisisobutyronitrile (30 g) premixed with ethyl acetate (1 Kg) were added 4 hours after the start of the reaction and again at 8 hours. The temperature was maintained at 55° C. throughout the reaction. The reaction was continued until complete. An antioxidant (61 g, IRGANOX™ 1010, Ciba-Geigy Corp.) and heptane (66.3 Kg) were added to the reactor and the contents mixed until homogeneous. The final copolymer had a measured inherent viscosity of 1.67 deciliter/g in ethyl acetate.
Aufarbeitung
- customThe mixture was deoxygenated
- additionazobisisobutyronitrile (30 g) premixed in ethyl acetate (1 Kg)
- additionwas charged to the reactor
- additionAdditional portions of azobisisobutyronitrile (30 g) premixed with ethyl acetate (1 Kg)
- additionwere added 4 hours
- customafter the start of the reaction
- waitagain at 8 hours
- temperatureThe temperature was maintained at 55° C. throughout the reaction
- additionthe contents mixed until homogeneous
Quellen und Nachweise
- ORD-Eintrag
- ord-31f64f604f5f4248a32fa774bf29c4a0
- Quelldatensatz
- uspto-grants-1996_12
- Patentnummer
- US05585111
Verknüpfte Notizen
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