echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Medical World News > The Synthetic Routes of 2-Chloro-6-methoxyquinoline-3-carboxaldehyde

    The Synthetic Routes of 2-Chloro-6-methoxyquinoline-3-carboxaldehyde

    • Last Update: 2023-05-08
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    2-Chloro-6-methoxyquinoline-3-carboxaldehyde is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products.
    The demand for this compound has been increasing steadily in recent years, making its synthetic routes an important area of research and development in the chemical industry.


    One of the most commonly used methods for the synthesis of 2-chloro-6-methoxyquinoline-3-carboxaldehyde is the reaction of 2-chloro-6-methoxyquinoline-3-carbaldehyde with oxalyl chloride in the presence of a catalyst such as DMF.
    This method involves the formation of an acyl chloride, which is then hydrolyzed to produce the desired carboxaldehyde.


    Another popular synthetic route for 2-chloro-6-methoxyquinoline-3-carboxaldehyde involves the reaction of 2-chloro-6-methoxyquinoline-3-carbaldehyde with ethyl chloroformate in the presence of a solvent such as DMF or DMSO.
    This method also involves the formation of an acyl chloride, which is then reduced to produce the desired carboxaldehyde.


    A third synthetic route for 2-chloro-6-methoxyquinoline-3-carboxaldehyde involves the reaction of 2-chloro-6-methoxyquinoline-3-carbaldehyde with formaldehyde and hydrochloric acid in the presence of a catalyst such as sodium hydroxide.
    This method involves the formation of an oxymalononitrile, which is then reduced to produce the desired carboxaldehyde.


    In addition to these synthetic routes, other methods for the synthesis of 2-chloro-6-methoxyquinoline-3-carboxaldehyde have also been reported in the literature.
    These include the use of grignard reagents, the reaction of 2-chloro-6-methoxyquinoline-3-carbaldehyde with aldehydes, and the use of transition metal catalysts.


    One of the advantages of the synthetic routes described above is the high yield of the desired product.
    These methods also offer good selectivity, allowing for the production of high-purity 2-chloro-6-methoxyquinoline-3-carboxaldehyde.


    Another advantage of these synthetic routes is the relatively low cost and ease of implementation.
    The use of readily available reagents and catalysts, as well as the mild reaction conditions, make these methods practical and economical for large-scale production.


    Overall, the synthetic routes for 2-chloro-6-methoxyquinoline-3-carboxaldehyde are an important area of research and development in the chemical industry.
    The demand for this compound is increasing, and new and more efficient methods for its synthesis are being Developed to meet this demand.
    These methods offer high yields, good selectivity, and low cost, making them practical and economical for large-scale production.
    As the field continues to evolve, it is likely that new and improved synthetic routes for 2-chloro-6-methoxyquinoline-3-carboxaldehyde will be developed, leading to a more efficient and cost-effective production process for this important intermediate.


    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.