Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Thiosulfate | HCID 24477 | — |
| Edukt | Metaperiodic acid | HCID 65185 | — |
| Edukt | 4-Nitrophenyl methyl sulfide | HCID 96109 | — |
| Katalysator | Iron chloride (FeCl3) | HCID 24380 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 1-(Methylsulfinyl)-4-nitrobenzene | HCID 305882 | — |
Reaktionsschritte
A suspension of 25.0 g (147.8 mmol) 1-methylsulfanyl-4-nitro-benzene and 0.69 g (4.2 mmol) iron(III) chloride (anhydrous) in 120 ml acetonitrile is treated with 36.0 g (158.1 mmol) periodic acid and stirred at room temperature. At the start of heat evolution, the mixture is transiently cooled with an ice-bath, so that the temperature does not rise above 30° C. After the heat evolution has subsided, the mixture is stirred at room temperature for a further 10 mins. The mixture is poured into a solution of 150 g sodium thiosulphate in 1000 ml ice-water and then extracted with DCM. The combined organic phases are washed with saturated NaCl solution, dried (Na2SO4), filtered and concentrated. The remaining residue is recrystallised from toluene. 23.6 g (128.0 mmol, corresponding to 86% of theor.) of the product is obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524724B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-cafb6242f564439da553abac38a251f3 |
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| Quellennotiz | uspto-grants-2013_09 |
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