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    Home > Active Ingredient News > Active Ingredient Products News > The Synthetic Routes of 5-BROMO-N-BUTYL-2-METHOXYBENZENESULFONAMIDE

    The Synthetic Routes of 5-BROMO-N-BUTYL-2-METHOXYBENZENESULFONAMIDE

    • Last Update: 2023-05-08
    • Source: Internet
    • Author: User
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    The Synthetic Routes of 5-BROMO-N-BUTYL-2-METHOXYBENZENESULFONAMIDE: An Overview in the Chemical Industry


    Introduction:
    5-Bromo-N-Butyl-2-Methoxybenzensulfonamide is an important pharmaceutical intermediate that is widely used in the production of various drugs.
    The demand for this compound has been steadily increasing in recent years due to its diverse range of applications in the pharmaceutical and chemical industries.
    As a result, several synthetic routes have been developed to produce 5-Bromo-N-Butyl-2-Methoxybenzensulfonamide in commercially viable quantities.
    In this article, we will discuss some of the most commonly used synthetic routes for the production of 5-Bromo-N-Butyl-2-Methoxybenzensulfonamide.


    Synthetic Route 1: The Mizoroki-Heck Reaction
    The Mizoroki-Heck reaction is one of the most commonly used synthetic routes for the production of 5-Bromo-N-Butyl-2-Methoxybenzensulfonamide.
    In this reaction, a halogenated alkene is reacted with a Grignard reagent in the presence of a palladium catalyst.
    The reaction proceeds through a transient metallocene intermediate, resulting in the formation of the desired product.


    Synthetic Route 2: The Stille Reaction
    The Stille reaction is another widely used synthetic route for the production of 5-Bromo-N-Butyl-2-Methoxybenzensulfonamide.
    In this reaction, a halogenated alkene is reacted with a phenylzinc halide in the presence of a copper catalyst.
    The reaction proceeds through a metallocene intermediate, resulting in the formation of the desired product.


    Synthetic Route 3: The Suzuki Reaction
    The Suzuki reaction is another attractive synthetic route for the production of 5-Bromo-N-Butyl-2-Methoxybenzensulfonamide.
    In this reaction, a halogenated arylboronic acid is reacted with a Grignard reagent in the presence of a palladium catalyst.
    The reaction proceeds through a transient metallocene intermediate, resulting in the formation of the desired product.


    Advantages and Limitations of the Synthetic Routes:
    Each of the synthetic routes for the production of 5-Bromo-N-Butyl-2-Methoxybenzensulfonamide has its own advantages and limitations.
    The Mizoroki-Heck reaction is highly efficient and can be performed in a single step, but it requires the use of expensive palladium catalysts.
    The Stille reaction is simple to perform and can be performed using inexpensive reagents, but it often results in a low yield of the desired product.
    The Suzuki reaction is also highly efficient and can be performed using inexpensive reagents, but it requires the use of a palladium catalyst.


    Conclusion:
    In conclusion, the synthetic routes for the production of 5-Bromo-N-Butyl-2-Methoxybenzensulfonamide are numerous, and each route has its own advantages and limitations.
    The Mizoroki-Heck reaction, the Stille reaction, and the Suzuki reaction are some of the most commonly used synthetic routes for the production of this compound.
    The choice of synthetic route will depend on several factors, including the availability of reagents, the cost of the reaction, and the desired yield of the product.
    As the demand for 5-Bromo-N-Butyl-2-Methoxybenzensulfonamide continues to increase in the pharmaceut


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