Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenol, 4-bromo-, 1-acetate | HCID 74726 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 3,5-Diacetoxy Styrene | HCID 11310559 | — |
| Katalysator | Tetrabutylammonium Chloride | HCID 70681 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Triacetylresveratrol | HCID 5962587 | — |
Reaktionsschritte
A flask equipped with magnetic stirrer was charged with 50 mg (0.23 mmol, 1 eq) of 3,5-diacetoxystyrene, 49 mg (0.23 mmol) of 4-acetoxybromobenzene, 46 mg (0.27 mmol) of NaHCO3 and 78 mg (0.54 mmol, 2.4 eq) of tetrabutylammoniumchloride. The reactants were suspended in 2 ml DMF and the mixture was flushed with argon and then evacuated. The argon flushing and evacuation procedure was carried out three times. The reaction was started by adding 0.76 mg of palladium acetate in 50 μl of de-aerated DMF (3 μmol, 1.5 mol %), and stirred at 100° C. for three hours. Work-up of the reaction mixture following the procedure of Example 5 gave (E)-3,4′,5-triacetoxystilbene.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07820848B2 |
|---|
| Quelldatensatz | uspto-grants-2010_10 |
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| ORD ID | ord-c1bbab8e0da74da3ae16839899640c2c |
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| Quellennotiz | uspto-grants-2010_10 |
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