Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Thiophenol | HCID 7969 | — |
| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | Picolyl chloride | HCID 23393 | — |
| Edukt | Cesium fluoride | HCID 25953 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-((Phenylthio)methyl)pyridine | HCID 194422 | — |
Reaktionsschritte
Thiophenol 2(2) (2.77 g, 0.025 mol), cesium carbonate (24.65 g, 0.075 mol) and catalytical amount of cesium fluoride were added successively to a solution of 2-chloromethylpyridine 6(1) (1.13 g, 0.017 mol) in absolute DMF (28 ml). The reaction mixture was stirred at 50-60° C. for 2 h in argon current and left for night at 20° C. Solvent was removed in vacuo, the residue was dissolved in water, the reaction product was extracted with CH2Cl2, dried over MgSO4, solvent was evaporated in vacuo. It gave 2-phenylsulphanylmethylpyridine 6(2), 3.2 g, (95%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08829002B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-732657db7ea443d1bfa53512ad456a36 |
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| Quellennotiz | uspto-grants-2014_09 |
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