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  2. Pyrrole - Wikipedia

    en.wikipedia.org/wiki/Pyrrole

    Pyrrole is an extremely weak base for an amine, with a conjugate acid pK a of −3.8. The most thermodynamically stable pyrrolium cation (C 4 H 6 N +) is formed by protonation at the 2 position. Substitution of pyrrole with alkyl substituents provides a more basic molecule—for example, tetramethylpyrrole has a conjugate acid pK a of +3.7.

  3. Hantzsch pyrrole synthesis - Wikipedia

    en.wikipedia.org/wiki/Hantzsch_pyrrole_synthesis

    A library of substituted pyrrole analogs can be quickly produced by using continuous flow chemistry (reaction times of around 8 min.). [10] The advantage of using this method, as opposed to the in-flask synthesis, is that this one does not require the work-up and purification of several intermediates, and could therefore lead to a higher ...

  4. Knorr pyrrole synthesis - Wikipedia

    en.wikipedia.org/wiki/Knorr_pyrrole_synthesis

    The Knorr pyrrole synthesis is a widely used chemical reaction that synthesizes substituted pyrroles (3). [ 1 ] [ 2 ] [ 3 ] The method involves the reaction of an α- amino - ketone (1) and a compound containing an electron-withdrawing group (e.g. an ester as shown) α to a carbonyl group (2) .

  5. Trofimov Reaction - Wikipedia

    en.wikipedia.org/wiki/Trofimov_Reaction

    The condensation reaction can be shown below: After the condensation, the pyrrole formation can proceed as normal. The Trofimov reaction can produce both N-H and N-vinyl pyrroles depending on the reaction conditions used. The N-vinyl pyrrole can be formed by the deprotonation of the pyrrole nitrogen which then attacks a second acetylene molecule.

  6. Pyrroline - Wikipedia

    en.wikipedia.org/wiki/Pyrroline

    Pyrrolines, also known under the name dihydropyrroles, are three different heterocyclic organic chemical compounds that differ in the position of the double bond.Pyrrolines are formally derived from the aromate pyrrole by hydrogenation. 1-Pyrroline is a cyclic imine, whereas 2-pyrroline and 3-pyrroline are cyclic amines.

  7. Organophosphine - Wikipedia

    en.wikipedia.org/wiki/Organophosphine

    For example, lithium diphenylphosphide is readily methylated with methyl iodide to give methyldiphenylphosphine: LiiP(C 6 H 5) 2 + CH 3 I → CH 3 P(C 6 H 5) 2 + LiI. Phosphine is a precursor to some tertiary phosphines by hydrophosphination of alkenes. For example, in the presence of basic catalysts PH 3 adds of Michael acceptors such as ...

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  9. Pyrrolidine - Wikipedia

    en.wikipedia.org/wiki/Pyrrolidine

    Pyrrolidine, also known as tetrahydropyrrole, is an organic compound with the molecular formula (CH 2) 4 NH. It is a cyclic secondary amine , also classified as a saturated heterocycle . It is a colourless liquid that is miscible with water and most organic solvents.