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    Home > Active Ingredient News > Study of Nervous System > The Synthetic Routes of Ergosterol

    The Synthetic Routes of Ergosterol

    • Last Update: 2023-05-12
    • Source: Internet
    • Author: User
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    Ergosterol is a naturally occurring sterol found in various fungi, and it has a wide range of applications in the chemical industry.
    It is used as an intermediate in the production of various chemicals, such as steroids, vitamins, and other pharmaceuticals.
    The synthetic routes for ergosterol have been developed over the years, and several methods are now available for its synthesis.
    In this article, we will discuss some of the most commonly used synthetic routes for ergosterol.


    1. The Mevinolin Route
      The Mevinolin route is one of the most commonly used methods for the synthesis of ergosterol.
      It involves the use of mevinolin, which is a plant sterol that is obtained from the seed of the Vernonia genre of plants.
      The mevinolin is treated with sodium hydroxide to remove the unreacted hydrocarbon chain, followed by treatment with an alcohol to form an ester.
      The ester is then reduced with hydrogen in the presence of a catalyst to form an aldehyde, which is then treated with a strong base to form an alcohol.
      The alcohol is then treated with chloroform and an aqueous solution of sodium hydroxide to form analkali-metanolic acid, which is then hydrolyzed to form ergosterol.
    2. The Swern Oxidation Route
      The Swern oxidation route is another commonly used method for the synthesis of ergosterol.
      It involves the use of swern oxidation, which is a chemical reaction in which a primary alcohol is treated with pyridine and hydrogen peroxide in the presence of a metal catalyst, such as palladium or platinum, to form an aldehyde.
      The aldehyde is then treated with sodium hydroxide and chloroform to form analkali-metanolic acid, which is then hydrolyzed to form ergosterol.
    3. The Gilman-Leland Oxidation Route
      The Gilman-Leland oxidation route is a chemical reaction in which a primary or secondary alcohol is treated with ozone and a Lewis acid, such as CuCl or AlCl3, in the presence of a solvent, such as water or ether, to form an aldehyde.
      The aldehyde is then treated with sodium hydroxide and chloroform to form analkali-metanolic acid, which is then hydrolyzed to form ergosterol.

    In conclusion, there are several synthetic routes available for the synthesis of ergosterol, and the choice of method depends on several factors, such as the availability of starting materials, the purity of the desired product, and the cost and efficiency of the synthesis.
    The Mevinolin route, the Swern oxidation route, and the Gilman-Leland oxidation route are three commonly used methods for the synthesis of ergosterol, and each method has its own advantages and disadvantages.


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