Oxidative cyclization of linoleic acid in the presence of hydrogen peroxide and phosphotungstic acid - Archive ouverte HAL
Article Dans Une Revue Molecular Catalysis Année : 2020

Oxidative cyclization of linoleic acid in the presence of hydrogen peroxide and phosphotungstic acid

Nahla Araji
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Gregory Chatel
Audrey Moores
  • Fonction : Auteur
  • PersonId : 1041352
Karine de Oliveira Vigier

Résumé

The synthesis of THF and tetrahydro-2H-pyrane is of interest due to the applications of such molecules as antitumour, pesticidal, antiprotozoal and antimicrobial agents for instance. Here, an original approach was performed to prepare these derivatives starting from linoleic acid in the presence of hydrogen peroxide and phosphotungstic acid in the absence of a phase transfer agent. A maximum cyclic compounds yield of 99% was obtained under mild conditions of temperature. A heterogeneous catalyst was synthesized by exchanging proton by Cs to obtain Cs2,3H0,7PW12O40 that was recycled up to 3 cycles. It is one of the best yield to these products observed in the literature from fatty acids.

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Catalyse
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Dates et versions

hal-03015077 , version 1 (19-11-2020)

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Nahla Araji, Gregory Chatel, Audrey Moores, François Jerome, Karine de Oliveira Vigier. Oxidative cyclization of linoleic acid in the presence of hydrogen peroxide and phosphotungstic acid. Molecular Catalysis, 2020, 493, pp.111084. ⟨10.1016/j.mcat.2020.111084⟩. ⟨hal-03015077⟩

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