Japp-Klingemann Synthesis

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Edwin Weber - One of the best experts on this subject based on the ideXlab platform.

  • Unusual Behaviour During the Route of a Japp-Klingemann Reaction
    Zeitschrift für Naturforschung B, 2010
    Co-Authors: Jan Marten, Wilhelm Seichter, Jörg Wagler, Edwin Weber
    Abstract:

    Performing a standard Japp-Klingemann Synthesis that involved diazotation of 2,6-dinitroaniline and reaction with pentane-2,4-dione in aqueous hydrochloric acid medium surprisingly yielded a mixture of the expected 2,6-dinitroand the unexpected 2-chloro-6-nitro-substituted hydrazones. This mixture was isolated as solid-solution crystals containing the components in an approximate ratio of 1 to 2. Based on both, selected compounds of comparison that show the aromatic ring substituents changed in position and intermediate diazonium salts, potential causal connections of the unusual behaviour during the route of the particular Japp-Klingemann reaction were studied. X-Ray crystal structures of the relevant compounds have been determined to support the discussion.

Jan Marten - One of the best experts on this subject based on the ideXlab platform.

  • Unusual Behaviour During the Route of a Japp-Klingemann Reaction
    Zeitschrift für Naturforschung B, 2010
    Co-Authors: Jan Marten, Wilhelm Seichter, Jörg Wagler, Edwin Weber
    Abstract:

    Performing a standard Japp-Klingemann Synthesis that involved diazotation of 2,6-dinitroaniline and reaction with pentane-2,4-dione in aqueous hydrochloric acid medium surprisingly yielded a mixture of the expected 2,6-dinitroand the unexpected 2-chloro-6-nitro-substituted hydrazones. This mixture was isolated as solid-solution crystals containing the components in an approximate ratio of 1 to 2. Based on both, selected compounds of comparison that show the aromatic ring substituents changed in position and intermediate diazonium salts, potential causal connections of the unusual behaviour during the route of the particular Japp-Klingemann reaction were studied. X-Ray crystal structures of the relevant compounds have been determined to support the discussion.

Wilhelm Seichter - One of the best experts on this subject based on the ideXlab platform.

  • Unusual Behaviour During the Route of a Japp-Klingemann Reaction
    Zeitschrift für Naturforschung B, 2010
    Co-Authors: Jan Marten, Wilhelm Seichter, Jörg Wagler, Edwin Weber
    Abstract:

    Performing a standard Japp-Klingemann Synthesis that involved diazotation of 2,6-dinitroaniline and reaction with pentane-2,4-dione in aqueous hydrochloric acid medium surprisingly yielded a mixture of the expected 2,6-dinitroand the unexpected 2-chloro-6-nitro-substituted hydrazones. This mixture was isolated as solid-solution crystals containing the components in an approximate ratio of 1 to 2. Based on both, selected compounds of comparison that show the aromatic ring substituents changed in position and intermediate diazonium salts, potential causal connections of the unusual behaviour during the route of the particular Japp-Klingemann reaction were studied. X-Ray crystal structures of the relevant compounds have been determined to support the discussion.

Jörg Wagler - One of the best experts on this subject based on the ideXlab platform.

  • Unusual Behaviour During the Route of a Japp-Klingemann Reaction
    Zeitschrift für Naturforschung B, 2010
    Co-Authors: Jan Marten, Wilhelm Seichter, Jörg Wagler, Edwin Weber
    Abstract:

    Performing a standard Japp-Klingemann Synthesis that involved diazotation of 2,6-dinitroaniline and reaction with pentane-2,4-dione in aqueous hydrochloric acid medium surprisingly yielded a mixture of the expected 2,6-dinitroand the unexpected 2-chloro-6-nitro-substituted hydrazones. This mixture was isolated as solid-solution crystals containing the components in an approximate ratio of 1 to 2. Based on both, selected compounds of comparison that show the aromatic ring substituents changed in position and intermediate diazonium salts, potential causal connections of the unusual behaviour during the route of the particular Japp-Klingemann reaction were studied. X-Ray crystal structures of the relevant compounds have been determined to support the discussion.