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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1163265Erstellt: 26. Oktober 2026

5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol → 5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol

https://huagongshe.com/reaction/1163265

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-DiolHCID 5056—
Edukt3,5-DihydroxybenzaldehydeHCID 94365—
Edukt4-IodophenylacetateHCID 141793—
Edukt1,3-Benzenediol, 5-ethenyl-HCID 12164063—
Produkt5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-DiolHCID 5056—
ProduktPiceatannolHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07820848B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-00134d72c1124357a29b76cff212c850
Quellennotizuspto-grants-2010_10