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    Home > Active Ingredient News > Antitumor Therapy > The Synthetic Routes of 6-(trifluoromethyl)-2,3-dihydro-1H-indol-5-ol

    The Synthetic Routes of 6-(trifluoromethyl)-2,3-dihydro-1H-indol-5-ol

    • Last Update: 2023-05-11
    • Source: Internet
    • Author: User
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    6-(Trifluoromethyl)-2,3-dihydro-1H-indol-5-ol, also known as 5H-2,3-oxazepin-5-amine, is a synthetic compound that has found wide applications in the chemical industry.
    It is used as an intermediate in the production of various chemicals, drugs, and pharmaceuticals.
    The synthetic routes of this compound have been extensively studied, and several methods have been developed to synthesize it in high yield and purity.


    One of the most commonly used synthetic routes for 6-(trifluoromethyl)-2,3-dihydro-1H-indol-5-ol is the Pictet-Spengler reaction.
    This reaction involves the condensation of phenylglyoxal with sodium hydroxide in the presence of a solvent such as water or ethanol.
    The reaction produces 5H-2,3-oxazepin-5-amine, which can be further transformed into the desired product using various chemical reactions.
    This method is relatively straightforward and simple, and it can be easily scaled up for industrial production.


    Another synthetic route for 6-(trifluoromethyl)-2,3-dihydro-1H-indol-5-ol is via the Grignard reaction.
    In this method, a Grignard reagent is prepared by the reaction of magnesium metal with an alkyl halide.
    The Grignard reagent is then treated with a base, such as sodium hydroxide, to form the corresponding sodium salt.
    This salt is then reacted with a suitable reagent to form the desired product.
    This method requires the use of specialized equipment and reagents, but it is highly efficient and can produce high yields of the target compound.


    In addition to the above methods, 6-(trifluoromethyl)-2,3-dihydro-1H-indol-5-ol can also be synthesized using other chemical reactions, such as the reduction of 6-(trifluoromethyl)indole-2,3-dione with lithium aluminum hydride or the condensation of 6-bromo-2,3-dihydro-1H-indol-5-ol with phenyl isocyanate.
    The choice of synthetic route depends on various factors, such as the availability of reagents, the scale of production, and the desired yield and purity of the final product.


    Once synthesized, 6-(trifluoromethyl)-2,3-dihydro-1H-indol-5-ol can be converted into a variety of chemicals and drugs.
    For example, it can be reduced to form 2,3-dihydro-1H-indol-5-ol, which is a key intermediate in the production of several antidepressant drugs.
    It can also be converted into 6-(trifluoromethyl)-2,3-dihydro-1H-indol-5-one, which is used in the production of anti-inflammatory drugs.
    The versatility of 6-(trifluoromethyl)-2,3-dihydro-1H-indol-5-ol makes it an important building block in the chemical industry.


    Overall, 6-(trifluoromethyl)-2,3-dihydro-1H-indol-5-ol is an important synthetic compound with a wide range of applications in the chemical industry.
    Its synthetic routes have been extensively studied, and various methods have been developed to synthesize it in high yield and purity.
    The compound can be converted into a variety of chemicals and drugs, making it an essential building block in the production of several pharmaceuticals.
    With ongoing research and development in the field, it is likely that new synthetic routes and applications for 6-(trifluoromethyl)-2,3-dihydro-1H-indol-5-ol will be discovered in the future.


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