Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 4-Nitrobenzenethiol | HCID 15809 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-Nitrophenyl methyl sulfide | HCID 96109 | 50,4% |
Reaktionsschritte
To a suspension of p-nitrothiophenol (20 g, 0.129 mol) in water (150 mL) was added an aqueous solution of sodium hydroxide (75 mL, 2 N) at room temperature. After the mixture was stirred for 15 minutes and cooled to 10° C., methyl iodide (57 g, 25 mL, 0.401 mol) was added slowly. The reaction mixture was allowed to warm to room temperature and stirred for 2.5 hours. The resulting mixture was extracted with diethyl ether (100 mL×3). The organic layers were combined, washed with water (200 mL) and brine (200 mL), dried over calcium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography to afford 11 g of 1-(methylsulfanyl)-4-nitrobenzene as a yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08871756B2 |
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| Quelldatensatz | uspto-grants-2014_10 |
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| ORD ID | ord-d7ccfdfe81114b4f9d7cad3ce0991d41 |
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| Quellennotiz | uspto-grants-2014_10 |
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