echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Drugs Articles > The Production Process of 2,3-Butanediol, 2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-, (2R,3R)-, methanesulfonate (1:1)

    The Production Process of 2,3-Butanediol, 2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-, (2R,3R)-, methanesulfonate (1:1)

    • Last Update: 2023-05-11
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    The production process of 2,3-Butanediol, 2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-, (2R,3R)-, methanesulfonate (1:1) involves several steps, including the synthesis of the precursor, the reaction with methanesulfonate, and the isolation of the final product.


    Step 1: Synthesis of the Precursor


    The first step in the production process of 2,3-Butanediol, 2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-, (2R,3R)-, methanesulfonate (1:1) is the synthesis of the precursor, which involves the reaction of 2,4-difluorophenyl amine with 1H-1,2,4-triazole in the presence of a Lewis acid catalyst, such as aluminum chloride.


    The reaction takes place in a suitable solvent, such as a homogeneous mixture of water and ethanol, at a temperature of around 50-60°C.
    The reaction mixture is then cooled to room temperature, and the precipitated solid is filtered and washed with water to remove any impurities.


    Step 2: Reaction with Methanesulfonate


    The next step in the production process of 2,3-Butanediol, 2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-, (2R,3R)-, methanesulfonate (1:1) is the reaction of the precursor with methanesulfonate, which is carried out in the presence of a Lewis acid catalyst, such as sulfuric acid.


    The reaction takes place in a suitable solvent, such as ethyl acetate, at a temperature of around 50-60°C.
    The reaction mixture is then cooled to room temperature, and the resulting precipitate is filtered and washed with ethyl acetate to remove any impurities.


    Step 3: Isolation of the Final Product


    The final step in the production process of 2,3-Butanediol, 2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-, (2R,3R)-, methanesulfonate (1:1) is the isolation of the final product, which involves the dissolution of the crude precipitate in a suitable solvent, such as ethyl acetate, and the subsequent crystallization of the product.


    The crystallized product is then filtered and washed with ethyl acetate to remove any impurities, and is dried under vacuum to remove any residual solvent.
    The final product is then subjected to further purification steps, such as high-performance liquid chromatography (HPLC), to remove any remaining impurities.


    Conclusion


    The production process of 2,3-Butanediol, 2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-, (2R,3R)-, methanesulfonate (1:1) involves the synthesis of the precursor, the reaction with methanesulfonate, and the isolation of the final product.
    The process requires the use of suitable solvents, Lewis acid catalysts, and purification steps to produce the final product in high purity.


    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.