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    Home > Active Ingredient News > Drugs Articles > The Synthetic Routes of 2-((2S,3S,4R,5R)-5-((S)-2,3-Bis((tert-butyldimethylsilyl)oxy)propyl)-4-methoxy-3-((phenylsulfonyl)methyl)tetrahydrofuran-2-yl)acetaldehyde

    The Synthetic Routes of 2-((2S,3S,4R,5R)-5-((S)-2,3-Bis((tert-butyldimethylsilyl)oxy)propyl)-4-methoxy-3-((phenylsulfonyl)methyl)tetrahydrofuran-2-yl)acetaldehyde

    • Last Update: 2023-05-10
    • Source: Internet
    • Author: User
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    Synthetic Routes of 2-((2S,3S,4R,5R)-5-((S)-2,3-Bis((tert-butyldimethylsilyl)oxy)propyl)-4-methoxy-3-((phenylsulfonyl)methyl)tetrahydrofuran-2-yl)acetaldehyde


    In the world of organic chemistry, the synthesis of new molecules is a constant pursuit, driven by the desire to create new compounds with unique and desirable properties.
    The process of synthesis involves the manipulation of building blocks, known as reagents, to create a new molecule, often through a series of chemical reactions.
    In this article, we will explore the synthetic routes of 2-((2S,3S,4R,5R)-5-((S)-2,3-Bis((tert-butyldimethylsilyl)oxy)propyl)-4-methoxy-3-((phenylsulfonyl)methyl)tetrahydrofuran-2-yl)acetaldehyde, a compound with a complex structure and intriguing properties.


    One of the most common synthetic routes for this compound is through the reaction of 2,3-bis((tert-butyldimethylsilyl)oxy)propyl acetate with 3-((phenylsulfonyl)methyl)tetrahydrofuran-2-one in the presence of a strong base such as sodium hydroxide.
    This reaction involves the nucleophilic substitution of the acetate group in the starting material for the oxygen atom in the phenylsulfonyl group, creating a new carbon-carbon bond.
    The product of this reaction is then treated with a base, such as sodium hydroxide, to hydrolyze the acetal group and create the aldehyde functional group.


    Another synthetic route for this compound involves the reaction of 2,3-bis((tert-butyldimethylsilyl)oxy)propyl chloride with 3-((phenylsulfonyl)methyl)tetrahydrofuran-2-one in the presence of a base such as pyridine.
    This reaction follows a similar mechanism to the previous route, with the nucleophilic substitution of the chloride group in the starting material for the oxygen atom in the phenylsulfonyl group, creating a new carbon-carbon bond.
    The product of this reaction is then treated with a base, such as pyridine, to hydrolyze the acetal group and create the aldehyde functional group.


    The synthesis of 2-((2S,3S,4R,5R)-5-((S)-2,3-Bis((tert-butyldimethylsilyl)oxy)propyl)-4-methoxy-3-((phenylsulfonyl)methyl)tetrahydrofuran-2-yl)acetaldehyde is a complex process that requires the use of specialized reagents and conditions.
    The compound itself is of interest due to its unique structure and potential applications in the field of organic chemistry.
    Further research and development may lead to the discovery of new synthetic routes and the creation of new compounds with similar properties.


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