Reaktion #53632

ord-9d0d135e03344dec9f4be50c80bf0de4

Reaktionsgleichung

CCCCC(CC)C(c1ccccc1)(c1ccccc1)[PH]([O-])([O-])[O-]
diphenyl-(2-ethylhexyl)phosphite
CC(C)(c1ccc(O)cc1)c1ccc(O)cc1
bisphenol-A
[Na]
sodium
CC(C)(c1ccc(O)cc1)c1ccc(O)cc1.CCCCCCCCOP([O-])[O-]
4,4′{-isopropylidenediphenol} octylphosphite

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas reduced to 90-100° C
  2. 2
    SonstigeThe phenol was then removed under vacuum (10 mm) over 2.5 hours
  3. 3
    workup.ADDITIONWhen the residual pressure dropped to 1 mm

Vorschrift

In a round bottom flask, 34.6 g (0.1 mol) of diphenyl-(2-ethylhexyl)phosphite, 22.8 g (0.1 mol) of bisphenol-A, and a catalytic quantity of metallic sodium (or alcoholate of an alkali metal) was heated at 180° C. under an atmosphere of nitrogen for one hour. The temperature was reduced to 90-100° C. The phenol was then removed under vacuum (10 mm) over 2.5 hours. When the residual pressure dropped to 1 mm, the reaction mass was subjected to vacuum for two more hours. The yield was quantitative. The phosphorus-31 NMR showed a series of peaks from 126 to 131 ppm.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06858662B2uspto-grants-2005_02