echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Medical World News > The Synthetic Routes of Ethyl 6-(trifluoromethyl)-3-pyridazinecarboxylate

    The Synthetic Routes of Ethyl 6-(trifluoromethyl)-3-pyridazinecarboxylate

    • Last Update: 2023-05-17
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    Ethyl 6-(trifluoromethyl)-3-pyridazinecarboxylate is a synthetic compound that has found wide applications in the chemical industry.
    This compound is commonly used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals.
    The synthetic routes for the preparation of this compound have been extensively studied, and several methods have been developed to synthesize it.
    In this article, we will discuss some of the most commonly used synthetic routes for the preparation of Ethyl 6-(trifluoromethyl)-3-pyridazinecarboxylate.


    1. The Grignard Reaction Route

    One of the most commonly used synthetic routes for the preparation of Ethyl 6-(trifluoromethyl)-3-pyridazinecarboxylate is the Grignard reaction route.
    In this route, a Grignard reagent is prepared by the reaction of magnesium metal with a halogenated alkene, such as 1,1,1,3,3,3-hexamethyltrifluoropropene.
    The Grignard reagent is then treated with a suitable nucleophile, such as methyl iodide, to form the desired carboxylate.
    The Grignard reaction is a versatile reaction that can be used to synthesize a wide variety of compounds, and it is known for its high yield and purity.
    This route is economical and scalable, making it a popular choice for industrial applications.


    1. The Friedel-Crafts Acylation Route

    Another commonly used synthetic route for the preparation of Ethyl 6-(trifluoromethyl)-3-pyridazinecarboxylate is the Friedel-Crafts acylation route.
    In this route, a primary or secondary amine is reacted with a halogenated derivative of an aromatic compound, such as benzene or toluene, in the presence of a Lewis acid catalyst, such as aluminum chloride.
    The reaction produces a nitro compound, which is then reduced to form the desired carboxylate.
    The Friedel-Crafts acylation route is a well-established method for the synthesis of aromatic carboxylates, and it is known for its high yield and purity.
    This route can be modified to synthesize various derivatives of Ethyl 6-(trifluoromethyl)-3-pyridazinecarboxylate, making it a versatile method for industrial applications.


    1. The Kharasch Synthesis Route

    The Kharasch synthesis is another synthetic route that can be used to prepare Ethyl 6-(trifluoromethyl)-3-pyridazinecarboxylate.
    In this route, a nitrile is treated with an alcohol in the presence of an acid catalyst, such as hydrochloric acid, to form an acetal.
    The acetal is then treated with a suitable reagent, such as sodium hydroxide, to form the desired carboxylate.
    The Kharasch synthesis is a simple and efficient method for the synthesis of carboxylates, and it is known for its high yield and purity.
    This route is economical and scalable, making it a popular choice for industrial applications.


    1. The Peterson Synthesis Route

    The Peterson synthesis is a synthetic route that can be used to prepare Ethyl 6-(trifluoromethyl)-3-pyridazinecarboxylate.
    In this route, a nitrile is treated with a primary or secondary amine in the presence of a strong acid catalyst, such as sulfuric acid, to form an amide.
    The amide is then treated with a suitable reagent, such as hydrogen sulfide, to form the desired carboxylate.
    The Peterson synthesis is a well-established method for the synthesis of carboxylates, and it


    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.