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Synthesis of Resveratrol and Resveratrol Trinicotinate

ZHANG Xue-jing, ZHU Jie, XIONG Xiao-yun, ZOU Yong*, LIN Hu i-zhen   

  1. 1. Guangzhou Institute of Chemistry, Chinese Academy of Sciences, Guangzhou Gua ngdong 510650, China;
    2. Department of Pharmacology, The Fourth Military Medical University, Xi′an Sh anxi 710032, China
  • Received:2003-11-06 Revised:2004-02-10 Online:2004-03-15 Published:2004-03-15
  • Contact: ZOU Yong*

Abstract: Aim To synthesize a new prodrug, resveratrol trinicotinate. Methods In presence of lithium and a catalytic amount of naphthalene, the reaction of p-methoxybenzyl trimethylsilyl ether and 3,5-dimethoxylbenzaldehyde gave resveratrol after a series of translation.Resveratrol trinicotinate was obtained by the reaction of resveratrol and nicotinoyl chloride hydrochloride. Results A mutual prodrug resveratrol trinicotinate was designed and synthesized. Conclusion A novel method for synthesis of resveratrol and resveratrol trinicotinate has been afforded.The E-isomer is selectivily obtained by dehydration of the compound 2 with KHSO4.

Key words: resveratrol, resveratrol, resveratrol trinicotinate, resveratrol trinicotinate, synthesis, synthesis

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