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    Home > Medical News > Medical World News > The Synthetic Routes of 4-Isoquinolinecarboxylic acid, ethyl ester

    The Synthetic Routes of 4-Isoquinolinecarboxylic acid, ethyl ester

    • Last Update: 2023-05-13
    • Source: Internet
    • Author: User
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    4-Isoquinolinecarboxylic acid, ethyl ester is an organic compound that is widely used in various industries, including the chemical, pharmaceutical, and cosmetic industries.
    The compound is known for its unique properties, which make it ideal for use in a variety of applications.
    In this article, we will explore the synthetic routes of 4-Isoquinolinecarboxylic acid, ethyl ester and their significance in the chemical industry.


    1. The Friedel-Crafts Acylation
      The Friedel-Crafts acylation is a common method used to synthesize 4-Isoquinolinecarboxylic acid, ethyl ester.
      In this process, a Grignard reagent is formed by the reaction of magnesium metal with an alkyl halide.
      The Grignard reagent is then treated with 4-Isoquinolinecarboxaldehyde in the presence of a Lewis acid catalyst, such as aluminum chloride, to form the desired ester.
    2. The Aldol Condensation
      Another synthetic route for 4-Isoquinolinecarboxylic acid, ethyl ester is the Aldol condensation.
      In this process, an aldol condensation is performed between 4-chloro-2-methylphenol and an equimolar amount of an aromatic aldehyde, such as benzaldehyde.
      The resulting intermediate is then treated with ethanol and sodium hydroxide to form the desired ester.
    3. The Hydrolysis of Acetates
      4-Isoquinolinecarboxylic acid can also be synthesized by the hydrolysis of acetates.
      In this process, the acetate is treated with water and a strong acid catalyst, such as hydrochloric acid, to form the desired carboxylic acid.
      The carboxylic acid is then esterified with ethanol to form the desired ester.
    4. The Halogenation of Benzene
      4-Isoquinolinecarboxylic acid can also be synthesized by the halogenation of benzene.
      In this process, benzene is treated with a halogenating agent, such as chloroform or bromoform, in the presence of a Lewis acid catalyst, such as aluminum chloride.
      The resulting intermediate is then treated with an aqueous solution of sodium hydroxide to form the desired carboxylic acid.
      The carboxylic acid is then esterified with ethanol to form the desired ester.

    In conclusion, there are various synthetic routes for 4-Isoquinolinecarboxylic acid, ethyl ester, and each method has its own advantages and disadvantages.
    The selection of a particular synthetic route depends on various factors, such as the availability of raw materials, the purity of the desired product, and the scale of production.
    However, regardless of the synthetic route, 4-Isoquinolinecarboxylic acid, ethyl ester remains an important compound in the chemical industry due to its unique properties and wide range of applications.


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