HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol → 5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol | HCID 5056 | — |
| Edukt | 3,5-Dihydroxybenzaldehyde | HCID 94365 | — |
| Edukt | 4-Iodophenylacetate | HCID 141793 | — |
| Edukt | 1,3-Benzenediol, 5-ethenyl- | HCID 12164063 | — |
| Produkt | 5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol | HCID 5056 | — |
| Produkt | Piceatannol | HCID 667639 | — |
Reaktionsschritte
Processes for the preparation of resveratrol have been disclosed, inter alia, in WO 01/60774 and Tetrahedron Letters 43 (2002) 597-598. The latter reference describes a process wherein resveratrol is prepared by a multistep reaction sequence starting with 3,5-dihydroxybenzaldehyde and involving a Heck reaction of 3,5-dihydroxystyrene with 4-acetoxy-iodobenzene in a yield of 70%. The process of the present invention utilizes a more readily available starting material and proceeds in less steps and superior yield, thus providing a technically more attractive approach to resveratrol and piceatannol and derivatives, such as esters, thereof.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07820848B2 |
| Quelldatensatz | uspto-grants-2010_10 |
| ORD ID | ord-00134d72c1124357a29b76cff212c850 |
| Quellennotiz | uspto-grants-2010_10 |