Réaction #1772057

ord-b4ab2e4211eb48caae28f7de1f8a23d1

Conditions de réaction

Température
100°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreto produce a crude product
  2. 2
    LavageThe crude product was washed twice with a 1N NaOH aqueous solution and once with distilled water
  3. 3
    LavageThe washed crude product
  4. 4
    Séchagewas then dried with magnesium sulfate
  5. 5
    FiltrationThen, the resultant was filtered
  6. 6
    AutreThe resultant was dried in a vacuum

Mode opératoire

1 mol of tertiary butylphenol, 2.2 mol of p-formaldehyde, and 1.1 mol of aniline were mixed and stirred without a solvent at 100° C. for 1 hour to produce a crude product. The crude product was washed twice with a 1N NaOH aqueous solution and once with distilled water. The washed crude product was then dried with magnesium sulfate. Then, the resultant was filtered. The resultant was dried in a vacuum to obtain the benzoxazine monomer represented by Formula 4. The benzoxazine monomer of Formula 4 was produced with a 95% yield. NMR spectrum of the benzoxazine monomer of Formula 4 is shown in FIG. 10.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08148028B2uspto-grants-2012_04