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    Home > Medical News > Medical World News > The Synthetic Routes of 2,6-DIFLUORO-3-(4,4,5,5-TETRAMETHYL-[1,3,2]-DIOXABOROLAN-2-YL)PYRIDINE

    The Synthetic Routes of 2,6-DIFLUORO-3-(4,4,5,5-TETRAMETHYL-[1,3,2]-DIOXABOROLAN-2-YL)PYRIDINE

    • Last Update: 2023-05-06
    • Source: Internet
    • Author: User
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    Synthetic routes of 2,6-difluoro-3-(4,4,5,5-tetramethyl-[1,3,2]-dioxaborolan-2-yl)pyridine are important in the chemical industry for several reasons.
    One of the primary reasons is the widespread use of this compound as an intermediate in the synthesis of various chemicals and pharmaceuticals.


    2,6-difluoro-3-(4,4,5,5-tetramethyl-[1,3,2]-dioxaborolan-2-yl)pyridine, commonly referred to as BDP, is a versatile building block that can be used to synthesize a variety of compounds.
    It has a unique structure that consists of a fluorinated pyridine ring attached to a boronic acid group.
    This makes it an attractive starting material for the synthesis of various compounds due to the unique properties of fluorine and boron.


    One of the primary synthetic routes for BDP is through a reaction known as Suzuki-Miyaura coupling.
    This reaction involves the reaction of a boronic acid derivative, such as 2-boronic acid-2,6-difluoropyridine, with a boronic acid derivative, such as 2-boronic acid-benzaldehyde.
    The resulting product is a boronate ester, which can be hydrolyzed to produce BDP.


    Another synthetic route for BDP is through the reaction of 2,6-difluoro-3-boropyridine with 2,2,2-trifluoroethyl 4-nitrophenylphosphonate.
    This reaction results in the formation of BDP as a minor product.


    BDP can also be synthesized through a reaction known as the Glaser-Hayama reaction.
    In this reaction, a phenylboronic acid derivative is reacted with a phenyl pyridine derivative in the presence of an excess of sodium hydroxide.
    The resulting product is a boronate ester, which can be reduced to produce BDP.


    In addition to these synthetic routes, BDP can also be synthesized through other methods, such as the reaction of 2,6-difluoro-3-boronphenylsilane with lithium hexamethyldisilylazide, or the reaction of 2,6-difluoro-3-boronic acid with sodium hydride.


    The synthetic routes of BDP are important in the chemical industry due to the widespread use of this compound as an intermediate in the synthesis of various chemicals and pharmaceuticals.
    Its unique structure, consisting of a fluorinated pyridine ring attached to a boronic acid group, makes it an attractive starting material for the synthesis of various compounds due to the unique properties of fluorine and boron.


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