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  2. Haloalkane - Wikipedia

    en.wikipedia.org/wiki/Haloalkane

    Azoalkanes may be reduced to primary amines by Staudinger reduction or lithium aluminium hydride. Amines may also be prepared from alkyl halides in amine alkylation, Gabriel synthesis and Delepine reaction, by undergoing nucleophilic substitution with potassium phthalimide or hexamine respectively, followed by hydrolysis. [citation needed]

  3. Gabriel synthesis - Wikipedia

    en.wikipedia.org/wiki/Gabriel_synthesis

    The Gabriel synthesis is a chemical reaction that transforms primary alkyl halides into primary amines.Traditionally, the reaction uses potassium phthalimide. [1] [2] [3] The reaction is named after the German chemist Siegmund Gabriel.

  4. Amine alkylation - Wikipedia

    en.wikipedia.org/wiki/Amine_alkylation

    Amine alkylation (amino-dehalogenation) is a type of organic reaction between an alkyl halide and ammonia or an amine. [1] The reaction is called nucleophilic aliphatic substitution (of the halide), and the reaction product is a higher substituted amine. The method is widely used in the laboratory, but less so industrially, where alcohols are ...

  5. Stieglitz rearrangement - Wikipedia

    en.wikipedia.org/wiki/Stieglitz_rearrangement

    The Stieglitz rearrangement of N-halogenated amines can be observed for chlorine [7] and bromine [8] substituted amines, often in combination with an organic base, such as sodium methoxide. [4] The need for a base is generally affiliated with the need for a deprotonation of the amine. [4] Stieglitz rearrangement N-haloamines

  6. Piperidine - Wikipedia

    en.wikipedia.org/wiki/Piperidine

    It is a colorless liquid with an odor described as objectionable, typical of amines. [6] The name comes from the genus name Piper , which is the Latin word for pepper . [ 7 ] Although piperidine is a common organic compound, it is best known as a representative structure element within many pharmaceuticals and alkaloids , such as natural ...

  7. Hydroamination - Wikipedia

    en.wikipedia.org/wiki/Hydroamination

    In organic chemistry, hydroamination is the addition of an N−H bond of an amine across a carbon-carbon multiple bond of an alkene, alkyne, diene, or allene. [1] In the ideal case, hydroamination is atom economical and green. [2] Amines are common in fine-chemical, pharmaceutical, and agricultural industries.

  8. Aminolysis - Wikipedia

    en.wikipedia.org/wiki/Aminolysis

    Another common example is the reaction of a primary amine or secondary amine with a carboxylic acid or with a carboxylic acid derivative to form an amide. This reaction is widely used, especially in the synthesis of peptides. On the simple addition of an amine to a carboxylic acid, a salt of the organic acid and base is obtained.

  9. Ethoxylation - Wikipedia

    en.wikipedia.org/wiki/Ethoxylation

    Although alcohols are by far the major substrate for ethoxylation, many nucleophiles are reactive toward ethylene oxide. Primary amines will react to give di-chain materials such as polyethoxylated tallow amine. The reaction of ammonia produces important bulk chemicals such as ethanolamine, diethanolamine, and triethanolamine.