Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Sodium Chloride | HCID 5234 | — |
| Edukt | 2,4-Dihydroxybenzaldehyde | HCID 7213 | — |
| Edukt | 3',4'-Dihydroxyacetophenone | HCID 14530 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | HCID 10424340 | HCID 10424340 | 75% |
Reaktionsschritte
At 0° C., hydrochloric acid (generated by dropwise addition of H2SO4 to NaCl) was bubbled in a two-necked flask containing 12 g (0.079 mol) of 3,4-dihydroxyacetophenone, 10.88 g (0.079 mol) of 2,4-dihydroxybenzaldehyde and 100 ml of ethyl acetate distilled beforehand. The product started to precipitate after 30 minutes. The bubbling was continued for another 1 hour and then the reaction was stopped. The solution was kept at −18° C. for 3 days and then it was filtered. The filtrate was evaporated and it was taken up in ether; the product precipitated. It was separated from the ether, dissolved in hot methanol and then it was added slowly to an equivalent volume of acetone. The solution was placed in a refrigerator and the product started to precipitate. After filtration, the filtrate was evaporated, dissolved in a minimum of methanol and then ether was added until a precipitate appeared. The procedure was thus repeated several times until precipitate no longer appeared. The purity of the 3′,4′,7-trihydroxyflavylium chloride precipitate thus obtained with a yield of 75% was checked by HPLC (high-performance liquid chromatography).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06241785B1 |
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| Quelldatensatz | uspto-grants-2001_06 |
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| ORD ID | ord-cd034231b3244a81ab36790ecbdf8386 |
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| Quellennotiz | uspto-grants-2001_06 |
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