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  2. Diethylaniline - Wikipedia

    en.wikipedia.org/wiki/Diethylaniline

    Diethylaniline is the organic compound with the molecular formula (C 2 H 5) 2 NC 6 H 5. It is a colorless liquid but commercial samples are often yellow. It is a precursor to several dyes and other commercial products.

  3. N-Ethyl-N-(2-chloroethyl)aniline - Wikipedia

    en.wikipedia.org/wiki/N-Ethyl-N-(2-chloroethyl...

    N-Ethyl-N-(2-chloroethyl)aniline is the organic compound with the formula C 6 H 5 N(Et)(CH 2 CH 2 Cl) (Et = ethyl). It is a low-melting colorless solid that is an alkylating agent. The compound is a precursor to several cationic azo dyes via reaction of the chloroethyl group with tertiary amines or pyridine followed by azo coupling.

  4. N-Methylaniline - Wikipedia

    en.wikipedia.org/wiki/N-Methylaniline

    N-Methylaniline (NMA) is an aniline derivative.It is an organic compound with the chemical formula C 6 H 5 NH(CH 3).The substance is a colorless viscous liquid, Samples turn brown when exposed to air.

  5. Indole - Wikipedia

    en.wikipedia.org/wiki/Indole

    The main industrial routes start from aniline via vapor-phase reaction with ethylene glycol in the presence of catalysts: In general, reactions are conducted between 200 and 500 °C. Yields can be as high as 60%. Other precursors to indole include formyltoluidine, 2-ethylaniline, and 2-(2-nitrophenyl)ethanol, all of which undergo cyclizations. [28]

  6. Larock indole synthesis - Wikipedia

    en.wikipedia.org/wiki/Larock_indole_synthesis

    Monguchi et al. also derived 2- and 2,3-substituted indoles without using LiCl. [5] The optimized Indole reaction uses 10% Pd/C (3.0 mol%) with 1.1 equivalent of NaOAc, and NMP at 110–130 °C. Monguchi et al. state that their optimized condition of the Larock indole synthesis without LiCl is a more mild, environmentally benign, and efficient ...

  7. Stevens rearrangement - Wikipedia

    en.wikipedia.org/wiki/Stevens_rearrangement

    The reaction mechanism of the Stevens rearrangement is one of the most controversial reaction mechanisms in organic chemistry. [4] Key in the reaction mechanism [5] [6] for the Stevens rearrangement (explained for the nitrogen reaction) is the formation of an ylide after deprotonation of the ammonium salt by a strong base.

  8. Elimination reaction - Wikipedia

    en.wikipedia.org/wiki/Elimination_reaction

    Elimination reaction of cyclohexanol to cyclohexene with sulfuric acid and heat [1] An elimination reaction is a type of organic reaction in which two substituents are removed from a molecule in either a one- or two-step mechanism. [2] The one-step mechanism is known as the E2 reaction, and the two-step mechanism is known as the E1 reaction ...

  9. Ketene cycloaddition - Wikipedia

    en.wikipedia.org/wiki/Ketene_cycloaddition

    Ketene cycloadditions proceed by a concerted, [2+2] cycloaddition mechanism. Ketenes, unlike most alkenes, can align antarafacially with respect to other alkenes. Thus, the suprafacial- antarafacial geometry required for concerted, thermal [2+2] cycloaddition can be achieved in reactions of ketenes. [4]