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    Home > Active Ingredient News > Drugs Articles > The Synthetic Routes of 4-(TRIFLUOROMETHYL)CYCLOHEXANONE

    The Synthetic Routes of 4-(TRIFLUOROMETHYL)CYCLOHEXANONE

    • Last Update: 2023-05-12
    • Source: Internet
    • Author: User
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    4-(TRIFLUOROMETHYL)CYCLOHEXANONE, commonly referred to as trifluoromethylcyclohexanone, is a synthetic chemical compound that is widely used in the chemical industry.
    It is a colorless liquid with a characteristic odor and is soluble in many organic solvents.
    The chemical formula for 4-(TRIFLUOROMETHYL)CYCLOHEXANONE is C8H10F3O.


    The synthetic routes for 4-(TRIFLUOROMETHYL)CYCLOHEXANONE can be broadly classified into two categories: conventional methods and newer methods.


    Conventional Methods:


    The first synthetic route for 4-(TRIFLUOROMETHYL)CYCLOHEXANONE was developed by Adolf von Baeyer in the 19th century.
    The traditional method involved the reduction of nitrobenzene using hydrogen in the presence of a metal catalyst, such as palladium or platinum.
    This method involved several steps and was relatively complex.


    Another conventional method involved the reduction of chloroacetophenone using hydrogen in the presence of a metal catalyst.
    This method was simplified by the use of metal catalysts, such as palladium or rhodium, which reduced the number of steps required for the synthesis.


    Newer Methods:


    In recent years, newer methods for the synthesis of 4-(TRIFLUOROMETHYL)CYCLOHEXANONE have been developed, which are simpler, more efficient, and less expensive than conventional methods.


    One such method involves the use of lithium aluminum hydride (LiAlH4) as a reducing agent for the reduction of chloroacetophenone.
    This method provides a one-step synthesis of 4-(TRIFLUOROMETHYL)CYCLOHEXANONE from chloroacetophenone and lithium aluminum hydride in the presence of a catalyst, such as tetrahydrofuran (THF) or 1,4-dioxane.


    Another newer method involves the use of a transition metal complex, such as ferric chloride or ferric sulfate, to reduce nitrobenzene to 4-(TRIFLUOROMETHYL)CYCLOHEXANONE.
    This method provides a one-step synthesis of the compound and can be carried out at room temperature, making it simpler and more efficient than conventional methods.


    Advantages of Synthesizing 4-(TRIFLUOROMETHYL)CYCLOHEXANONE:


    4-(TRIFLUOROMETHYL)CYCLOHEXANONE has a wide range of applications in various industries, such as the pharmaceutical, cosmetics, and agrochemical industries.
    It is also used as a starting material in the production of various chemical intermediates.


    The synthesis of 4-(TRIFLUOROMETHYL)CYCLOHEXANONE has several advantages.
    It can be used as a versatile building block for the synthesis of other chemical compounds, and its unique properties make it an ideal candidate for various applications.
    Additionally, the ease of synthesis and availability of the starting materials make it a cost-effective option for industrial production.


    Conclusion:


    4-(TRIFLUOROMETHYL)CYCLOHEXANONE is an important synthetic chemical compound that has a wide range of applications in the chemical industry.
    The synthetic routes for the compound can be broadly classified into conventional methods and newer methods, with newer methods being simpler, more efficient, and less expensive than conventional methods.
    The synthesis of 4-(TRIFLUOROMETHYL)CYCLOHEXANONE has several advantages, such as its versatility as a building block for the synthesis of other chemical compounds and its cost-effectiveness.


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