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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163265Generated: October 26, 2026

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

https://huagongshe.com/reaction/1163265

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-DiolHCID 5056—
Reactant3,5-DihydroxybenzaldehydeHCID 94365—
Reactant4-IodophenylacetateHCID 141793—
Reactant1,3-Benzenediol, 5-ethenyl-HCID 12164063—
Product5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-DiolHCID 5056—
ProductPiceatannolHCID 667639—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820848B2
Source datasetuspto-grants-2010_10
ORD IDord-00134d72c1124357a29b76cff212c850
Source noteuspto-grants-2010_10