Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Nitrogen | HCID 947 | — |
| Edukt | Disilathiane, 1,1,1,3,3,3-hexamethyl- | HCID 76920 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Edukt | HCID 67128699 | HCID 67128699 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 86664919 | HCID 86664919 | — |
Reaktionsschritte
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), hexamethyldisilthiane (8.9 mL, 42.31 mmol) was added dropwise to a solution of NaOMe (2.35 g, 42.31 mmol) in dry DMF (35 mL) and the reaction mixture was stirred at rt for 15 min. This dark blue solution was then added to a solution of [5-(2-methyl-[1,3]dioxolan-2-yl)-thiophen-2-yl]-acetonitrile (3.27 g, 16.93 mmol) in DMF (30 mL) and the reaction mixture was stirred for 2 days at rt. Water (100 mL) was then added and the mixture was extracted twice with EA (100 mL). The combined org. phases were dried over MgSO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (1:1 hept-EA) gave the title compound as a yellow oil. TLC: rf (1:1 hept-EA)=0.35. LC-MS-conditions 02: tR=0.81 min, [M+H]+=244.38.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08674111B2 |
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| Quelldatensatz | uspto-grants-2014_03 |
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| ORD ID | ord-b94bf6f2887142f1bda88a4df95f6717 |
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| Quellennotiz | uspto-grants-2014_03 |
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