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Solvent-free synthesis of novel para-menthane-3,8-diol ester derivatives from citronellal using a polymer-supported scandium triflate catalyst.


ABSTRACT: The use of natural resources as a chemical feedstock for the synthesis of added-value products is gaining interest; as such we report an environmentally friendly method for the synthesis of para-menthane-3,8-diol from natural citronellal oil in 96% yield, under solvent free aqueous conditions. The acylation of para-menthane-3,8-diol with various acid anhydrides over polymer-supported scandium triflate (PS-Sc(OTf)3) catalyst was subsequently developed, where both hydroxy groups of para-menthane-3,8-diol could be simultaneous acylated under mild reaction conditions to form the corresponding diesters in good yields. The advantages of this method include a simple procedure from natural resources, using solvent-free reaction conditions.

SUBMITTER: Mafu L 

PROVIDER: S-EPMC5082460 | biostudies-other | 2016

REPOSITORIES: biostudies-other

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Solvent-free synthesis of novel <i>para</i>-menthane-3,8-diol ester derivatives from citronellal using a polymer-supported scandium triflate catalyst.

Mafu Lubabalo L   Zeelie Ben B   Watts Paul P  

Beilstein journal of organic chemistry 20160919


The use of natural resources as a chemical feedstock for the synthesis of added-value products is gaining interest; as such we report an environmentally friendly method for the synthesis of <i>para</i>-menthane-3,8-diol from natural citronellal oil in 96% yield, under solvent free aqueous conditions. The acylation of <i>para</i>-menthane-3,8-diol with various acid anhydrides over polymer-supported scandium triflate (PS-Sc(OTf)<sub>3</sub>) catalyst was subsequently developed, where both hydroxy  ...[more]

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