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  2. Reduction of nitro compounds - Wikipedia

    en.wikipedia.org/wiki/Reduction_of_nitro_compounds

    Catalytic hydrogenation using platinum(IV) oxide (PtO 2) [23] or Raney nickel [24] Iron metal in refluxing acetic acid [25] Samarium diiodide [26] Raney nickel, platinum on carbon, or zinc dust and formic acid or ammonium formate [6] α,β-Unsaturated nitro compounds can be reduced to saturated amines by: Catalytic hydrogenation over palladium ...

  3. Hydrogenation of carbon–nitrogen double bonds - Wikipedia

    en.wikipedia.org/wiki/Hydrogenation_of_carbon...

    In chemistry, the hydrogenation of carbon–nitrogen double bonds is the addition of the elements of dihydrogen (H 2) across a carbon–nitrogen double bond, forming amines or amine derivatives. [1] Although a variety of general methods have been developed for the enantioselective hydrogenation of ketones, [ 2 ] methods for the hydrogenation of ...

  4. Amide reduction - Wikipedia

    en.wikipedia.org/wiki/Amide_reduction

    Catalytic hydrogenation can be used to reduce amides to amines; however, the process often requires high hydrogenation pressures and reaction temperatures to be effective (i.e. often requiring pressures above 197 atm and temperatures exceeding 200 °C). [1]

  5. Reductive amination - Wikipedia

    en.wikipedia.org/wiki/Reductive_amination

    An example of a homogeneous catalytic system is the reductive amination of ketones done with an iridium catalyst. [20] Homogenous Iridium (III) catalysts have been shown to be effective in the reductive amination of carboxylic acids , which in the past has been more difficult than aldehydes and ketones. [ 16 ]

  6. Nitrile reduction - Wikipedia

    en.wikipedia.org/wiki/Nitrile_reduction

    The catalytic hydrogenation of nitriles is often the most economical route available for the production of primary amines. [3] Catalysts for the reaction often include group 10 metals such as Raney nickel , [ 4 ] [ 5 ] [ 6 ] palladium black , or platinum dioxide . [ 1 ]

  7. Baylis–Hillman reaction - Wikipedia

    en.wikipedia.org/wiki/Baylis–Hillman_reaction

    For example, in the three-component coupling of aldehydes, amines, and activated alkenes, the aldehyde reacts with the amine to produce an imine prior to forming the aza-MBH adduct, as in the reaction of aryl aldehydes, diphenylphosphinamide, and methyl vinyl ketone, in the presence of TiCl 4, triphenylphosphine, and triethylamine: [19]

  8. Hydrogenolysis - Wikipedia

    en.wikipedia.org/wiki/Hydrogenolysis

    The hydrogen sulfide is subsequently recovered in an amine treater and finally converted to elemental sulfur in a Claus process unit. In those industries, desulfurization process units are often referred to as hydrodesulfurizers (HDS) or hydrotreaters (HDT). Catalysts are based on molybdenum sulfide containing smaller amounts of cobalt or ...

  9. Hofmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Hofmann_rearrangement

    The Hofmann rearrangement (Hofmann degradation) is the organic reaction of a primary amide to a primary amine with one less carbon atom. [1] [2] [3] The reaction involves oxidation of the nitrogen followed by rearrangement of the carbonyl and nitrogen to give an isocyanate intermediate.