Water → (E)-1-(2,4,6-triiodophenoxy)-3,7-dimethyl-2,6-octadiene

HRID 53493

Reaktionsgleichung

Reaktionsgleichung von HRID 53493
[CH:1]1[C:2]([I:10])=[CH:3][C:4]([I:9])=[C:5]([OH:8])[C:6]=1[I:7].C(=O)([O-])[O-].[K+].[K+].[CH2:17](Br)/[CH:18]=[C:19](/[CH2:21][CH2:22][CH:23]=[C:24]([CH3:26])[CH3:25])\[CH3:20].O>CN(C)C=O>[I:7][C:6]1[CH:1]=[C:2]([I:10])[CH:3]=[C:4]([I:9])[C:5]=1[O:8][CH2:17]/[CH:18]=[C:19](\[CH3:20])/[CH2:21][CH2:22][CH:23]=[C:24]([CH3:26])[CH3:25]

Komponenten

6

Edukt 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 118622,4,6-TriiodophenolHCID 53658672,6-Octadiene, 1-bromo-3,7-dimethyl-, (2E)-

Produkt 1

HCID 15343331(E)-1-(2,4,6-triiodophenoxy)-3,7-dimethyl-2,6-octadieneAusbeute 87 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

A mixture of triiodophenol (10.0 g, 21.2 mmol), milled potassium carbonate (3.1 g, 22.5 mmol, 1.06 eq) and geranyl bromide (4.0 ml, 20.2 mmol) in dimethyl formamide (25 ml) was heated to 50° C. for 2 hrs and cooled. The mixture was poured into 300 ml of water and extracted with ethyl acetate. The ethyl acetate extract was filtered through a short pad of silica gel, then alumina, eluting with ethyl acetate-hexanes (1:1). The eluent was concentrated under high vacuum to give the product in 87% yield as an oil.

Aufarbeitung

  1. temperaturecooled
  2. extractionextracted with ethyl acetate
  3. extractionThe ethyl acetate extract
  4. filtrationwas filtered through a short pad of silica gel
  5. washalumina, eluting with ethyl acetate-hexanes (1:1)
  6. concentrationThe eluent was concentrated under high vacuum
  7. customto give the product in 87% yield as an oil

Quellen und Nachweise

ORD-Eintrag
ord-e22a45abcb974474bdf8c81aa359d759
Quelldatensatz
uspto-grants-1997_04
Patentnummer
US05620677

Verknüpfte Notizen

Wird geladen…