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Acrylonitrile → Methyl Acrylamidoglycolate Methyl Ether Acrylonitrile

HRID 2260475
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2260475
[CH3:1][O:2][CH:3]([NH:8][C:9](=[O:12])[CH:10]=[CH2:11])[C:4]([O:6][CH3:7])=[O:5].[C:13](#[N:16])[CH:14]=[CH2:15]>CO>[CH3:1][O:2][CH:3]([NH:8][C:9](=[O:12])[CH:10]=[CH2:11])[C:4]([O:6][CH3:7])=[O:5].[C:13](#[N:16])[CH:14]=[CH2:15]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 7855AcrylonitrileHCID 156893Methyl acrylamidoglycolate methyl ether

Produkt 1

HCID 131719224Methyl Acrylamidoglycolate Methyl Ether Acrylonitrile

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To a 5 liter 3-neck round bottom flask were added 233.6 grams (1.35 mole) of methyl acrylamidoglycolate methyl ether (MAGME™), 71.6 grams (1.35 mole) of acrylonitrile, and 246.8 grams of methanol solvent. The comonomer molar mix in this Example was 50:50. The flask was equipped with a water condenser, an Argon inlet and an Argon outlet to a bubbler to ensure that a positive Argon flow was maintained in the reaction vessel throughout the polymerization period. The mixture was mechanically stirred and sparged with Argon at ambient temperature for 2 hours to dissolve the monomers and displace oxygen. To the resulting solution were added 3.05 grams (0.0186 mole) of azobisisobutyrylnitrile initiator, and the stirred solution was warmed to and maintained at 60° C. for 24 hours by means of a hot water bath. The polymer solution was next rotoevaporated to dryness leaving the solid polymer which after vacuum oven drying for 24 hours at 40° C. at about 1 millimeters Hg amounted to 284 grams (93.0 percent of theory). This polymer was used without further purification as a positive charge adjuvant in Liquid Toner 4 prepared in Example VII.

Aufarbeitung

  1. customThe flask was equipped with a water condenser, an Argon inlet and an Argon outlet to a bubbler
  2. temperaturewas maintained in the reaction vessel throughout the polymerization period
  3. customsparged with Argon at ambient temperature for 2 hours
  4. dissolutionto dissolve the monomers
  5. temperaturethe stirred solution was warmed to and
  6. customleaving the solid polymer which after vacuum oven
  7. customdrying for 24 hours at 40° C. at about 1 millimeters Hg
  8. customThis polymer was used without further purification as
  9. additiona positive charge
  10. customprepared in Example VII

Quellen und Nachweise

ORD-Eintrag
ord-b2936bc743a348899cf8086c96f7c7c8
Quelldatensatz
uspto-grants-1995_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05478688

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