Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Di-p-tolyl sulphide | HCID 69294 | — |
| Edukt | 2-Iodoxybenzoic acid | HCID 108794 | — |
| Katalysator | Tetraethylammonium Bromide | HCID 6285 | — |
| Lösungsmittel | Chloroform water | HCID 22418719 | — |
| Produkt | Methyl phenyl sulfoxide | HCID 14516 | 99,9% |
Reaktionsschritte
To a stirred suspension of iodoxybenzoic acid (3.7 g, 13.2 mmol, 1.1 eq) in 100:1 CHCl3/H2O (25 mL) was added tetraethylammonium bromide (TEAB) (126 mg, 5 mol %), followed by the addition of p-tolyl sulfide (1.66 g, 12 mmol) in one portion. The mixture was stirred at room temperature for approximately 30 minutes until consumption of sulfide was observed (TLC, hexanes/EtOAc 1/1). The residual solids were removed by filtration and washed with CHCl3 (40 mL). The combined filtrate was washed successively with saturated aq. NaHCO3 (30 mL), saturated aq. NaCl (30 mL), dried over sodium sulfate, and concentrated to provide the crude product. Purification by silica gel column chromatography (50% hexanes/EtOAc elution) afforded the title compound (1.68 g, yield 91%). 1H NMR (300 MHz, CDCl3) δ 7.52 (d, J=8.4 Hz, 2H), 7.32 (d, J=8.4 Hz, 2H), 2.71 (s, 3H), 2.42 (s, 3H); ESI-MS m/z 154.7 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07915443B2 |
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| Quelldatensatz | uspto-grants-2011_03 |
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| ORD ID | ord-dae94bc90b4e40c9bfccf2a358742dc0 |
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| Quellennotiz | uspto-grants-2011_03 |
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