Reaktion #78025

ord-db5f8f3c860240cb9161dd66c55b5231

Reaktionsgleichung

C=C(C)c1ccccc1
α-methyl styrene
C=C(C)c1ccccc1C
isopropenyltoluene
Cc1ccccc1
toluene
C=C(C)c1ccccc1.C=C(C)c1ccccc1C
α-methylstyrene isopropenyltoluene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONmixed while boron trifluoride phenol complex
  2. 2
    workup.ADDITIONwas slowly added
  3. 3
    Temperaturthe material was then cooled under dry ice
  4. 4
    workup.ADDITIONNext, alkali was added to inactivate and
  5. 5
    Sonstigeremove the catalyst
  6. 6
    Einengenconcentrated
  7. 7
    Sonstigeto remove the solvent and unreacted monomer

Vorschrift

250 g α-methyl styrene (99.8% purity), 250 g isopropenyltoluene, and 500 g toluene were introduced into a three-mouthed flask, and mixed while boron trifluoride phenol complex was slowly added, and the material was then cooled under dry ice and acetone solvent and reacted for 3 hr at 20° C. Next, alkali was added to inactivate and remove the catalyst, and concentrated to remove the solvent and unreacted monomer, and α-methylstyrene-isopropenyltoluene copolymer was obtained as a residue. This polymer was designated Polymer B3, and its physical properties are listed in Table 2.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06709798B2uspto-grants-2004_03