Reaktion #216074

ord-870cecd120934980957fd3dd7b0cac14

Reaktionsgleichung

O
water
Oc1c(I)cc(I)cc1I
triiodophenol
[H-].[Na+]
sodium hydride
CC(CCOS(C)(=O)=O)OS(C)(=O)=O
1,3-bis-(methanesulfonyloxy) butane
CC(CCOc1c(I)cc(I)cc1I)Oc1c(I)cc(I)cc1I
desired product
Ausbeute 54.0%
CC(CCOc1c(I)cc(I)cc1I)Oc1c(I)cc(I)cc1I
1,3-Bis-(2,4,6-Triiodophenoxy)-butane
Ausbeute 54.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was heated to 90° C. for 6 hours
  2. 2
    Temperaturafter cooling
  3. 3
    workup.WAITto stand overnight
  4. 4
    SonstigeThe precipitated solid was collected
  5. 5
    Sonstigedried

Vorschrift

A mixture of triiodophenol (5.78 g, 12.3 mmol) and sodium hydride (0.49 g, 60% dispersion, 12.3 mmol) in DMF (15 ml) was stirred at room temperature for 1 hour and then a solution of 1,3-bis-(methanesulfonyloxy) butane (1.37 g, 5.58 mmol) in DMF (5 ml) was added. The mixture was heated to 90° C. for 6 hours and then poured into water after cooling. Ethyl acetate was added and the mixture was allowed to stand overnight. The precipitated solid was collected and dried to give 3.0 g (54%) of the desired product, Mp 173°-175° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05466435uspto-grants-1995_11