Reaktion #81762

ord-0bddb144ab1d491b81ab3a9d61a86613

Reaktionsgleichung

CCCCCCCCCCCCCC(C)Oc1c(I)cc(I)cc1I
2-(2,4,6-triiodophenoxy)-pentadecane
CS(=O)(=O)[O-]
mesylate
CCCCCCC(O)CC
3-nonanol
Oc1c(I)cc(I)cc1I
triiodophenol
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCCCCCCCCCCCCC(C)Oc1c(I)cc(I)cc1I
2-(2,4,6-triiodophenoxy)-pentadecane
CCCCCCC(CC)Oc1c(I)cc(I)cc1I
3-(2,4,6-Triiodophenoxy)-nonane
Ausbeute 67.3%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto provide a light brown oil

Vorschrift

The mesylate of 3-nonanol (11.5 g, 51.9 mmol), triiodophenol (24.5 g, 51.9 mmol) and potassium carbonate (7.18 g, 51.9 mmol) were reacted in dry DMF (200 ml) as per 2-(2,4,6-triiodophenoxy)-pentadecane except at an oil bath temperature of 87° C. for 16 hrs. The reaction was processed as for 2-(2,4,6-triiodophenoxy)-pentadecane to provide a light brown oil. Flash column chromatography (silica, hexanes) provided 3-(2,4,6-Triiodophenoxy)-nonane (20.9 g, 67%) as a clear viscous oil.

Quelle

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