echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Antitumor Therapy > The Synthetic Routes of Carmofur

    The Synthetic Routes of Carmofur

    • Last Update: 2023-05-01
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    Carmofur is a chemical compound commonly used as a intermediate in the production of dyes, pigments, and other chemical products.
    The synthetic routes for Carmofur can vary depending on the starting materials and the desired product properties.
    The following are some of the common synthetic routes for Carmofur.


    1. Direct Nitration of Anisole

    One of the most common methods for the synthesis of Carmofur involves the direct nitration of anisole in the presence of a strong nitrating agent such as nitric acid.
    The reaction is typically carried out in a mixture of water and an organic solvent such as acetone or ethyl acetate.
    The reaction is exothermic, and careful temperature control is required to prevent excessive heating.


    1. Kharasch Route

    An alternative synthetic route involves the reduction of anisaldehyde using hydrogen in the presence of a noble metal catalyst such as palladium or platinum.
    The reaction is typically carried out at high pressure and low temperature to prevent the unwanted formation of byproducts.


    1. Fischer Indole Synthesis

    Another method for the synthesis of Carmofur involves the Fischer indole synthesis, which involves the reaction of anisole with tryptamine in the presence of an acid catalyst such as sulfuric acid.
    The reaction produces a mixture of indoles, which can be separated and purified to yield Carmofur.


    1. Hydrogenation of Indigo

    Carmofur can also be synthesized by the hydrogenation of indigo, a blue dye molecule.
    The reaction is typically carried out in the presence of a heterogeneous catalyst such as palladium on barium sulfate.
    The reaction produces a mixture of indoles, which can be separated and purified to yield Carmofur.


    1. Direct Coupling of P-Tolualdehyde and Aniline

    Carmofur can also be synthesized by the direct coupling of P-tolualdehyde and aniline in the presence of a strong acid catalyst such as sulfuric acid.
    The reaction is typically carried out in an organic solvent such as chloroform or dichloromethane.


    In conclusion, the synthetic routes for Carmofur vary depending on the starting materials and the desired product properties.
    The methods outlined above are some of the most commonly used synthetic routes for Carmofur, but there are many other methods that can be used depending on the specific requirements of the manufacturing process.


    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.