JOURNAL of the Tunisian Chemical Society

serving the Research, the Education and the Industry

Nouvelle méthode de préparation de complexants du ferIII et synthèse ameliorée de l’intermédiaire pyrocatéchol monobenzyléther

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A new synthetic route is reported for siderophores APn having pyrocatechol groups located α to each carboxylic acid of a α,ω-linear diacid. The use of a benzyl group for protecting a phenolic hydroxide allows an easy deprotection by hydrogenolysis and gives a better yield for the multistep synthesis. An improved synthetic procedure for preparing the intermediate 2-benzyloxyphenol (pyrocatechol monobenzylether), by solid-liquid phase transfer catalysis, is reported (K2CO3, Aliquat, xylene; yield = 75%).

M. Ismaïl, A. Zinelabidine, F. Mhenni, R. Gallo

siderophores, protecting group, hydrogenolysis, ether cleavage, Phase Transfer Catalysis (PTC)

Pages 1591-1598

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