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    Home > Active Ingredient News > Active Ingredient Products News > The Synthetic Routes of 4-(2-HYDROXYETHYLSULFAMOYL)PHENYLBORONIC ACID

    The Synthetic Routes of 4-(2-HYDROXYETHYLSULFAMOYL)PHENYLBORONIC ACID

    • Last Update: 2023-05-08
    • Source: Internet
    • Author: User
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    4-(2-Hydroxyethylsulfamoyl)phenylboronic acid is an important intermediate in the synthesis of various chemicals and pharmaceuticals.
    The compound has a wide range of applications in various industries, particularly in the chemical and pharmaceutical industries.
    The demand for this compound has increased significantly over the past few years, and as a result, various synthetic routes have been developed to synthesize it.
    In this article, we will discuss some of the commonly used synthetic routes for the synthesis of 4-(2-hydroxyethylsulfamoyl)phenylboronic acid.


    One of the most commonly used synthesis routes is the synthesis of 4-(2-hydroxyethylsulfamoyl)phenylboronic acid via the Borkman reaction.
    The Borkman reaction is a well-established reaction in organic chemistry that involves the reaction of boric acid with anhydrous ammonia.
    In the first step, boric acid is reacted with excess anhydrous ammonia to form borane primary amines.
    In the second step, the primary amine is reacted with 4-chlorophenylboronic acid, and the product is then hydrolyzed to produce 4-(2-hydroxyethylsulfamoyl)phenylboronic acid.


    Another commonly used synthesis route for 4-(2-hydroxyethylsulfamoyl)phenylboronic acid is the synthesis of the compound via the synthesis of 4-aminophenylboronic acid.
    In this process, 4-aminophenylboronic acid is synthesized using conventional methods such as the reduction of 4-chlorophenylboronic acid with lithium aluminum hydride.
    Once the 4-aminophenylboronic acid is synthesized, it is then converted to 4-(2-hydroxyethylsulfamoyl)phenylboronic acid through a series of chemical reactions.


    In recent years, catalytic hydrogenation has emerged as a popular synthesis route for 4-(2-hydroxyethylsulfamoyl)phenylboronic acid.
    This process involves the reduction of 4-nitrophenylboronic acid using palladium on barium sulfate as a catalyst.
    The product is then hydrolyzed to produce 4-(2-hydroxyethylsulfamoyl)phenylboronic acid.
    This process is more environmentally friendly than the previously used methods and is also more cost-effective.


    In addition to the above-mentioned synthesis routes, 4-(2-hydroxyethylsulfamoyl)phenylboronic acid can also be synthesized via the synthesis of 4-(2-nitroethylsulfamoyl)phenylboronic acid.
    This process involves the reaction of 4-amino-2-nitrophenylboronic acid with sodium hydroxide in the presence of a base catalyst such as sodium carbonate.
    The product is then hydrolyzed to produce 4-(2-hydroxyethylsulfamoyl)phenylboronic acid.


    In conclusion, the synthesis of 4-(2-hydroxyethylsulfamoyl)phenylboronic acid has been a subject of extensive research in the chemical and pharmaceutical industries.
    The demand for this compound has increased significantly over the years, and as a result, various synthetic routes have been developed to synthesize it.
    Some of the commonly used synthetic routes include the synthesis of the compound via the Borkman reaction, the synthesis of 4-aminophenylboronic acid, the synthesis of the compound via catalytic hydrogenation, and the synthesis of 4-(2-nitroethylsulfamoyl)phenylboronic acid.
    Each of these synthesis routes has its advantages and disadvantages, and the choice of synthesis


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