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    Home > Active Ingredient News > Drugs Articles > The Synthetic Routes of Tris[3-(hydroxy-κO)-2-methyl-4H-pyran-4-onato-κO4]iron

    The Synthetic Routes of Tris[3-(hydroxy-κO)-2-methyl-4H-pyran-4-onato-κO4]iron

    • Last Update: 2023-05-11
    • Source: Internet
    • Author: User
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    Synthetic routes of Tris[3-(hydroxy-κO)-2-methyl-4H-pyran-4-onato-κO4]iron: A Comprehensive Review


    Introduction:


    Tris[3-(hydroxy-κO)-2-methyl-4H-pyran-4-onato-κO4]iron, commonly referred to as Fe(III)(OS3H2O)(H2O)3, is a synthetic compound with a unique structure and promising applications in areas such as catalysis and energy storage.
    The synthesis of this compound involves several steps, and the choice of route depends on the desired product properties and the availability of starting materials.
    In this article, we will review some of the most commonly used synthetic routes for Tris[3-(hydroxy-κO)-2-methyl-4H-pyran-4-onato-κO4]iron, including the traditional method and newer, more efficient approaches.


    Traditional Synthetic Route:


    The traditional synthetic route for Tris[3-(hydroxy-κO)-2-methyl-4H-pyran-4-onato-κO4]iron involves the condensation of salicylic aldehyde with sodium phenylphosphinate, followed by treatment with a strong base to generate the iron(III) salt.
    The reaction sequence is shown below:


    salicylic aldehyde + phenylphosphinate <ilde; NaOH + H3O+ salicylate <ilde; Fe(III) + H2O


    This route is well-established and has been used for decades to synthesize this compound.
    However, it is a multi-step process that requires careful control of reaction conditions to ensure product purity.


    Improved Synthetic Routes:


    In recent years, several improved synthetic routes for Tris[3-(hydroxy-κO)-2-methyl-4H-pyran-4-onato-κO4]iron have been developed, offering higher yields, shorter reaction times, and more environmentally friendly conditions.
    One of the most popular approaches is the hydrothermal method, which involves the condensation of salicylate with iron(III) chloride in the presence of a hydroxyl donor such as sodium hydroxide.
    The reaction proceeds in aqueous media at relatively low temperature and pressure, and the product can be easily isolated by filtration and washing with water.


    Another recently developed route is the one-pot hydrothermal-alkaline hydrolysis method, which combines the benefits of hydrothermal synthesis with those of alkaline hydrolysis.
    In this method, a mixture of salicylate, iron(III) chloride, and a hydroxyl donor such as sodium hydroxide is heated in an autoclave under hydrothermal conditions.
    After the reaction is complete, the product is isolated by filtration and washing with water, and then treated with concentrated hydrochloric acid to remove any remaining iron(III) chloride.


    Advantages and Limitations:


    The improved synthetic routes for Tris[3-(hydroxy-κO)-2-methyl-4H-pyran-4-onato-κO4]iron offer several advantages over the traditional method.
    They are generally more efficient, with higher yields and shorter reaction times, and can be performed using more environmentally friendly conditions, such as aqueous media and moderate temperatures and pressures.
    However, these routes also have some limitations.
    For example, they may require additional steps, such as filtration and washing, to isolate the product, and the choice of hydroxyl donor can have a significant impact on the product properties.


    Conclusion:


    Tris[3-(hydroxy-κO)-2-methyl-4H-pyran-4-onato-κO4]iron is an important synthetic compound with applications in areas such as catalysis and energy storage.
    The traditional synthetic route, which involves condensation of salicylic aldehyde with sodium phenylphosphinate followed by treatment with a strong base, is well-established but requires careful


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