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    Home > Medical News > Medical Products News > The Synthetic Routes of Ethanone, 1-(2-amino-5-chlorophenyl)-2,2,2-trifluoro-, hydrochloride (1:1)

    The Synthetic Routes of Ethanone, 1-(2-amino-5-chlorophenyl)-2,2,2-trifluoro-, hydrochloride (1:1)

    • Last Update: 2023-04-30
    • Source: Internet
    • Author: User
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    Ethanone, 1-(2-amino-5-chlorophenyl)-2,2,2-trifluoro-, hydrochloride (1:1) is an organic compound that is commonly used in the pharmaceutical and chemical industries.
    It is a synthetic chemical that is derived from a variety of starting materials through a series of chemical reactions.
    The synthetic routes of ethanone involve a combination of chemical reactions such as nucleophilic substitution, electrophilic substitution, and elimination, among others.


    One of the most common synthetic routes to ethanone involves the reaction of 2-amino-5-chlorophenol with 2,2,2-trifluoroacetyl chloride in the presence of a strong acid catalyst.
    The reaction causes the nucleophilic substitution of the chloride ion in the acetyl chloride with the amino group in the 2-amino-5-chlorophenol, resulting in the formation of an intermediate carbocation.
    This intermediate is then protonated by the strong acid catalyst to form the final product, 1-(2-amino-5-chlorophenyl)-2,2,2-trifluoro-ethanone.


    Another synthetic route to ethanone involves the reaction of 2-fluoro-5-nitrophenyl acetate with sodium hydroxide in the presence of a solvent such as ether.
    The reaction causes the electrophilic substitution of the acetate ion with the sodium hydroxide, leading to the formation of the intermediate nitroso compound.
    This intermediate is then reduced using hydrogen gas in the presence of a metal catalyst such as palladium on coal to form the final product, 1-(2-amino-5-chlorophenyl)-2,2,2-trifluoro-ethanone.


    In a third synthetic route, ethanone can be synthesized by the reaction of 2,2,2-trifluoro-1-(2-aminophenyl)ethanone with chloroformic acid in the presence of a catalyst such as aluminum chloride.
    The reaction causes the elimination of water from the intermediate carbocation to form the final product, 1-(2-amino-5-chlorophenyl)-2,2,2-trifluoro-ethanone.


    In all of these synthetic routes, the final product is typically purified by recrystallization, which involves dissolving the crude product in a solvent such as ethanol or methanol and allowing the solvent to slowly evaporate, leaving behind pure crystals of the final product.


    The synthetic routes of ethanone, 1-(2-amino-5-chlorophenyl)-2,2,2-trifluoro-, hydrochloride (1:1) involve a variety of chemical reactions and purification methods.
    These routes are commonly used in the pharmaceutical and chemical industries to synthesize this important organic compound.
    The synthetic routes involve the use of strong acids, metal catalysts, and solvents, among others, to form the final product.
    The product is typically purified by recrystallization to provide a pure form of the compound that can be used in a variety of applications.



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