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    Home > Medical News > Medical World News > The Synthetic Routes of 8-Bromoacetylquinoline hydrobromide

    The Synthetic Routes of 8-Bromoacetylquinoline hydrobromide

    • Last Update: 2023-05-08
    • Source: Internet
    • Author: User
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    8-Bromoacetylquinoline hydrobromide is an important chemical intermediate used in the production of various pharmaceuticals, agrochemicals, and other industrial products.
    This compound has a complex molecular structure, which makes its synthesis challenging.
    There are several synthetic routes available for the preparation of 8-bromoacetylquinoline hydrobromide, each with its own advantages and disadvantages.


    The most common synthetic route for the preparation of 8-bromoacetylquinoline hydrobromide involves the reaction of acetylquinoline with bromine in the presence of a solvent such as carbon tetrachloride or chloroform.
    In this process, acetylquinoline is first treated with bromine in the presence of a Lewis acid catalyst such as zinc chloride or aluminum chloride.
    The resulting mixture is then treated with additional bromine, and the reaction is allowed to proceed for several hours.
    The resulting product is then extracted with a solvent such as ether or benzene and treated with a base such as sodium hydroxide to produce the hydrobromide salt of 8-bromoacetylquinoline.


    Another synthetic route involves the reaction of acetylanthranilic acid with bromine in the presence of an acid catalyst such as sulfuric acid.
    In this process, acetylanthranilic acid is treated with bromine in the presence of the acid catalyst and the reaction is allowed to proceed for several hours.
    The resulting product is then treated with a base such as sodium hydroxide to produce the hydrobromide salt of 8-bromoacetylquinoline.


    A third synthetic route involves the reaction of acetylaniline with bromine in the presence of a solvent such as carbon tetrachloride.
    In this process, acetylaniline is treated with bromine in the presence of a Lewis acid catalyst such as zinc chloride or aluminum chloride, and the reaction is allowed to proceed for several hours.
    The resulting product is then extracted with a solvent such as ether or benzene and treated with a base such as sodium hydroxide to produce the hydrobromide salt of 8-bromoacetylquinoline.


    Each of these synthetic routes has its own advantages and disadvantages.
    The first route is relatively simple and easy to perform, but it requires the use of toxic reagents such as bromine and zinc chloride.
    The second route is more environmentally friendly, as it does not require the use of toxic reagents, but it is more complex and requires the use of specialized equipment.
    The third route is also relatively simple and easy to perform, but it requires the use of a toxic solvent such as carbon tetrachloride.


    The selection of a specific synthetic route for the preparation of 8-bromoacetylquinoline hydrobromide will depend on a variety of factors, including the availability of starting materials, the desired yield, and the purity of the final product.
    In addition, the cost and availability of the necessary equipment and reagents must also be taken into account.


    Overall, the synthetic routes for the preparation of 8-bromoacetylquinoline hydrobromide are numerous, and each has its own advantages and disadvantages.
    The selection of a specific route will depend on the specific needs and circumstances of the manufacturer.
    However, regardless of the route chosen, the production of 8-bromoacetylquinoline hydrobromide requires careful attention to detail, and must be performed in a well-equipped laboratory by trained and knowledgeable personnel.


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