Reaktionsgleichung
[CH2:1]([S:3]SCC)[CH3:2].[C:7]1([CH3:16])[CH:12]=[CH:11][C:10]([S:13]([O-:15])=[O:14])=[CH:9][CH:8]=1.[Na+].II>>[C:7]1([CH3:16])[CH:12]=[CH:11][C:10]([S:13](=[O:15])([S:3][CH2:1][CH3:2])=[O:14])=[CH:9][CH:8]=1Komponenten
4
Versuchsvorschrift
The reaction was carried out using 0.60 mL (4.87 mmoL) of diethyl disulfide, 2.78 g (15.6 mmoL) of sodium p-toluenesulfinate, 2.47 g (9.74 mmoL) of iodine in accordance with the method of Reference Example 3, and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=8:1) to obtain 2.11 g of the heading compound as a colorless oily substance (yield 100%).
Aufarbeitung
- customthe obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=8:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-e4712a18d0d144cbaaf6ae12dbb30cd8
- Quelldatensatz
- uspto-grants-2012_07
- Patentnummer
- US08222407B2
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