Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hexane | HCID 8058 | — |
| Edukt | 2,5-Dibromothiophene | HCID 18453 | — |
| Edukt | 4-Fluoro-N-methoxy-N-methylbenzamide | HCID 14069347 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-Bromo-5-(4-fluorophenylcarbonyl)thiophene | HCID 19963306 | 86% |
Reaktionsschritte
A solution of 2,5-dibromothiophene (19.23 g, 75.5 mmol) in anhydrous THF (400 mL) was treated at -78° C. under nitrogen with a 2.5M solution of n-butyllithium in hexane (30.0 mL, 75.5 mmol). The resulting solution was stirred for 45 minutes at -78° C. and then transferred by cannula into a cold (-78° C.) solution of N-methoxy-N-methyl-4-fluorobenzamide (12.57 g, 68.6 mmol), prepared as in step 1, in anhydrous THF (300 mL) with siring. After 30 minutes at -78° C., the reaction was quenched by the addition of a saturated solution of NH4Cl (15 mL) and poured into ethanol (350 mL) containing 10% HCl (140 mL). The mixture was partitioned between brine and 1:1 ether and dichloromethane. The organic layer was dried over Na2SO4 and concentrated in vacuo. The residue was crystallized from pentane to give 16.8 g (86%) of 2-bromo-5-(4-fluorophenylcarbonyl)thiophene.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05616596 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-4623753a4d434523892abc50b4ff3f3f |
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| Quellennotiz | uspto-grants-1997_04 |
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