Reaktionsgleichung
CS(OC(CCCCCCC)C)(=O)=O.C1C(I)=CC(I)=C(O)C=1I.C(=O)([O-])[O-].[K+].[K+].[I:31][C:32]1[CH:53]=[C:52]([I:54])[CH:51]=[C:50]([I:55])[C:33]=1[O:34][CH:35]([CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43]CCCCCC)[CH3:36]>CN(C=O)C>[I:31][C:32]1[CH:53]=[C:52]([I:54])[CH:51]=[C:50]([I:55])[C:33]=1[O:34][CH:35]([CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43])[CH3:36]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The 2-methanesulfonyloxynonane (22.8 g, 102 mmol), triiodophenol (48.8 g, 103 mmol) and potassium carbonate (14.2 g, 103 mmol) were reacted in DMF (206 ml) as per 2-(2,4,6-triiodophenoxy)pentadecane except at an oil bath temperature of 82° C. for 14 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 2-(2,4,6-triiodophenoxy)nonane (40.8 g, 68.0%).
Aufarbeitung
- customto provide a light brown oil
Quellen und Nachweise
- ORD-Eintrag
- ord-5924d4a5d885450cb80faddba131a647
- Quelldatensatz
- uspto-grants-1997_03
- Patentnummer
- US05607660
Verknüpfte Notizen
Wird geladen…