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New efficient catalysts based on hydrotalcite for synthesis of sandalwood-type fragrances

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F24%3A43928000" target="_blank" >RIV/60461373:22310/24:43928000 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0920586123004297?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0920586123004297?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.cattod.2023.114405" target="_blank" >10.1016/j.cattod.2023.114405</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    New efficient catalysts based on hydrotalcite for synthesis of sandalwood-type fragrances

  • Original language description

    The presented study focuses on the development of metal-modified bifunctional catalysts based on hydrotalcites (HT) and their utilization for the „one-pot“ synthesis of 2-methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-enol, also known as Santalinol. Such fragrance has a strong scent of sandalwood and is used in the perfume and cosmetics industry. The synthesis of Santalinol involves two steps: the aldol condensation of campholenic aldehyde with propanal to form 2-methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-enal (santalinal), followed by selective hydrogenation. Three hydrotalcites with different magnesium-aluminium ratios ranging from 2 to 3 were prepared and tested for aldol condensation. Among them, the most active catalyst was modified with a metal using the impregnation method and various metal precursors. The modification using palladium (II) acetylacetonate solution in toluene proved to be the most advantageous. An efficient bifunctional catalyst was prepared, consisting of a hydrotalcite with a magnesium-aluminium ratio of 2.5 and 0.1 wt% of palladium for Santalinol synthesis. Under optimal conditions in a one-pot reaction, a 40% conversion of campholenic aldehyde was achieved after aldol condensation, with a selectivity of 86% towards santalinal. During the hydrogenation step, a selectivity of up to 75% towards Santalinol, relative to the formed santalinal, was observed. © 2023 Elsevier B.V.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10401 - Organic chemistry

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2024

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    CATALYSIS TODAY

  • ISSN

    0920-5861

  • e-ISSN

    1873-4308

  • Volume of the periodical

    427

  • Issue of the periodical within the volume

    Neuveden

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    11

  • Pages from-to

    nestránkováno

  • UT code for WoS article

    001097144800001

  • EID of the result in the Scopus database

    2-s2.0-85175053825