Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetone | HCID 180 | — |
| Edukt | tert-Butanol | HCID 6386 | — |
| Edukt | 2-Bromo-1-thiophen-3-yl-butan-1-one | HCID 59598618 | — |
| Edukt | HCID 178461630 | HCID 178461630 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | 2-Bromo-1-thiophen-3-yl-butan-1-one | HCID 59598618 | — |
| Produkt | 5-Thiophen-3-yl-heptane-2,4-dione | HCID 59598638 | — |
Reaktionsschritte
EtMgBr (6.69 ml, 13 mmol, 2 M in ethyl ether) in benzene (10 ml) was cooled to zero degrees C., and tBuOH (1.28 ml, 13 mmol) was slowly added. The reaction mixture was stirred at zero degrees C. for 5 minutes, then acetone (530 ul, 7 mmol) was added, followed by a solution of 2-Bromo-1-thiophen-3-yl-butan-1-one (1.3 g, 6 mmol) in 3 ml benzene via cannula. The reaction mixture was heated to reflux for 1 hour, and acetone (250 ul) was added. The reaction mixture was heated 2 hours more at reflux. The reaction was cooled, quenched with 1 N HCl (10 ml), extracted three times with diethyl ether, washed brine, and dried over magnesium sulfate. The solvent was removed in vacuo and the residue chromatographed (5% ethyl acetate/hexanes) to give 247 mg of 2-Bromo-1-thiophen-3-yl-butan-1-one starting material and 520 mg of 5-Thiophen-3-yl-heptane-2,4-dione, 44%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08524725B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-bc19b9a175a54cfebeeaa16f982df689 |
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| Quellennotiz | uspto-grants-2013_09 |
|---|