Sodium Iodide → 6-Phenyl-1-hexyl iodide
Reaktionsgleichung
CS(O[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)(=O)=O.[I-:18].[Na+]>CC(C)=O>[C:12]1([CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][I:18])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To 6-phenylhex-1-yl methylsulfonate (4.55 g; 17.3 mmol) dissolved in acetone (100 ml) is added sodium iodide (2.5 g; 173 mmol) and the reaction mixture is heated 2 hours at reflux. The reaction mixture is then concentrated to dryness and partitioned between ether and water. The organic phase is separated, dried, concentrated to dryness and purified with silica chromatography using 10 EtOAc/90 petroleum ether to give 6-phenyl-1-hexyl iodide as a colorless oil which is used directly in Step F.
Aufarbeitung
- temperaturethe reaction mixture is heated 2 hours
- temperatureat reflux
- concentrationThe reaction mixture is then concentrated to dryness
- custompartitioned between ether and water
- customThe organic phase is separated
- customdried
- concentrationconcentrated to dryness
- custompurified with silica chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-8f17090b939c4349a5cc3b771a243771
- Quelldatensatz
- uspto-grants-1996_10
- Patentnummer
- US05561143
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