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  2. Phenylhydrazine - Wikipedia

    en.wikipedia.org/wiki/Phenylhydrazine

    Phenylhydrazine was the first hydrazine derivative characterized, reported by Hermann Emil Fischer in 1875. [7] [8] He prepared it by reduction of a phenyl diazonium salt using sulfite salts. Fischer used phenylhydrazine to characterize sugars via formation of hydrazones known as osazones with the sugar aldehyde. He also demonstrated in this ...

  3. Hydrazines - Wikipedia

    en.wikipedia.org/wiki/Hydrazines

    Hydrazines (R 2 N−NR 2) are a class of chemical compounds with two nitrogen atoms linked via a covalent bond and which carry from one up to four alkyl or aryl substituents. . Hydrazines can be considered as derivatives of the inorganic hydrazine (H 2 N−NH 2), in which one or more hydrogen atoms have been replaced by hydrocarbon grou

  4. Fischer indole synthesis - Wikipedia

    en.wikipedia.org/wiki/Fischer_indole_synthesis

    The reaction of a (substituted) phenylhydrazine with a carbonyl (aldehyde or ketone) initially forms a phenylhydrazone which isomerizes to the respective enamine (or 'ene-hydrazine'). After protonation , a cyclic [3,3]-sigmatropic rearrangement occurs producing a diimine .

  5. Hydrazone - Wikipedia

    en.wikipedia.org/wiki/Hydrazone

    When derived from hydrazine itself, hydrazones condense with a second equivalent of a carbonyl to give azines: [11] R 2 C=N−NH 2 + R 2 C=O → R 2 C=N−N=CR 2 + H 2 O. Hydrazones are intermediates in the Wolff–Kishner reduction. Hydrazones are reactants in hydrazone iodination, the Shapiro reaction, and the Bamford–Stevens reaction to ...

  6. Osazone - Wikipedia

    en.wikipedia.org/wiki/Osazone

    Osazone formation was developed by Emil Fischer, [3] who used the reaction as a test to identify monosaccharides.. The formation of a pair of hydrazone functionalities involves both oxidation and condensation reactions. [4]

  7. Olin Raschig process - Wikipedia

    en.wikipedia.org/wiki/Olin_Raschig_process

    The Olin Raschig process is a chemical process for the production of hydrazine.The main steps in this process, patented by German chemist Friedrich Raschig in 1906 and one of three reactions named after him, are the formation of monochloramine from ammonia and hypochlorite, and the subsequent reaction of monochloramine with ammonia towards hydrazine. [1]

  8. Hydrazine - Wikipedia

    en.wikipedia.org/wiki/Hydrazine

    Hydrazine is an inorganic compound with the chemical formula N 2 H 4.It is a simple pnictogen hydride, and is a colourless flammable liquid with an ammonia-like odour.Hydrazine is highly hazardous unless handled in solution as, for example, hydrazine hydrate (N 2 H 4 ·xH 2 O).

  9. Acetone azine - Wikipedia

    en.wikipedia.org/wiki/Acetone_azine

    Download as PDF; Printable version ... hydrazine manufacturing processes. Synthesis. Acetone azine can be prepared from acetone and hydrazine : [3] 2 (CH 3) 2 CO + N ...