Reaktion #81761

ord-4966d7dfdd4c4daeb429ef5e22629560

Reaktionsgleichung

O
water
Oc1c(I)cc(I)cc1I
2,4,6-triiodophenol
O=C([O-])[O-].[K+].[K+]
potassium carbonate
BrCCC(c1ccccc1)c1ccccc1
3,3-diphenylpropyl bromide
Ic1cc(I)c(OCCC(c2ccccc2)c2ccccc2)c(I)c1
solid
Ausbeute 48.2%
Ic1cc(I)c(OCCC(c2ccccc2)c2ccccc2)c(I)c1
3,3-Diphenyl-1-(2,4,6-triiodophenoxy)propane
Ausbeute 48.2%

Reaktionsbedingungen

Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled
  2. 2
    Temperaturwas heated at 60° C. for 24 hrs
  3. 3
    TemperaturThe mixture was then cooled
  4. 4
    SonstigeThe product was purified by silica gel chromatography (2.5% ethyl acetate-hexanes)
  5. 5
    Sonstigefollowed by recrystallization from hexanes

Vorschrift

A mixture of 2,4,6-triiodophenol (0.78 g, 1.65 mmol) and potassium carbonate (0.25 g, 1.82 mmol, 1.1 eq) in 5 ml of dimethylformamide was heated at 60° C. for 1 hr, cooled and then 3,3-diphenylpropyl bromide (0.5 g, 1.82 mmol) was added. After stirring for 30 minutes at room temperature the mixture was heated at 60° C. for 24 hrs. The mixture was then cooled, poured into water and the crude product was isolated by ethyl acetate extraction. The product was purified by silica gel chromatography (2.5% ethyl acetate-hexanes) followed by recrystallization from hexanes to give 0.53 g (48%) of a solid. Mp: 120°-121° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05620677uspto-grants-1997_04