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Aminocarbene mechanism of the formation of a tertiary amine in nitrile hydrogenation on a palladium catalyst

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F13%3A43895904" target="_blank" >RIV/60461373:22310/13:43895904 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1007/s11144-012-0497-2" target="_blank" >http://dx.doi.org/10.1007/s11144-012-0497-2</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s11144-012-0497-2" target="_blank" >10.1007/s11144-012-0497-2</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Aminocarbene mechanism of the formation of a tertiary amine in nitrile hydrogenation on a palladium catalyst

  • Original language description

    The hydrogenation of an aliphatic nitrile, molecules of which do not bear hydrogen atoms on the alpha-carbon with respect to the nitrile group, has been studied to gain a deeper insight into the mechanism of the heterogeneously catalyzed hydrogenation ofnitriles. Hydrogenations were performed in the liquid phase on a Pd/C catalyst at a reaction temperature of 110 A degrees C and a hydrogen pressure of 5 MPa. In the hydrogenation of trimethylacetonitrile in the presence of a lower aliphatic N,N-dialkylamine (e.g., diethylamine), the formation of a mixed tertiary amine, dialkylneopentylamine, was observed. Experiments have shown that the disproportionation reactions of the amines present are not responsible for its formation. Since the corresponding enamine incorporating a double bond in the neopentyl chain cannot be derived from the dialkylneopentylamine, the formation of the dialkylneopentylamine cannot be explained in terms of the enamine theory of the formation of a tertiary amine d

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GPP106%2F10%2FP441" target="_blank" >GPP106/10/P441: What causes the differences in catalytic properties of metals in the nitrile hydrogenation?</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2013

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Reaction Kinetics Mechanisms and Catalysis

  • ISSN

    1878-5190

  • e-ISSN

  • Volume of the periodical

    108

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    15

  • Pages from-to

    91-105

  • UT code for WoS article

    000313370800008

  • EID of the result in the Scopus database