echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Medical World News > The Synthetic Routes of 2(1H)-Pyrimidinone, 5-acetyl-4-methyl- (9CI)

    The Synthetic Routes of 2(1H)-Pyrimidinone, 5-acetyl-4-methyl- (9CI)

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

    Introduction


    2(1H)-Pyrimidinone, 5-acetyl-4-methyl- (9CI) is an organic compound that has gained significant attention in the chemical industry due to its diverse range of applications.
    This compound is commonly used as an intermediate in the synthesis of various chemicals, drugs, and other industrial products.
    In this article, we will discuss the various synthetic routes that are used to manufacture 2(1H)-Pyrimidinone, 5-acetyl-4-methyl- (9CI).


    Synthetic Routes of 2(1H)-Pyrimidinone, 5-acetyl-4-methyl- (9CI)


    1. The Mannich Reaction

    The Mannich reaction is one of the most commonly used methods for the synthesis of 2(1H)-Pyrimidinone, 5-acetyl-4-methyl- (9CI).
    In this reaction, a compound called ketone or aldehyde is reacted with formaldehyde and a primary or secondary amine in the presence of a base.
    The reaction produces a Mannich base, which can be further converted into 2(1H)-Pyrimidinone, 5-acetyl-4-methyl- (9CI) through a series of chemical reactions.


    1. The Grignard Reaction

    The Grignard reaction is another synthetic route that can be used to manufacture 2(1H)-Pyrimidinone, 5-acetyl-4-methyl- (9CI).
    In this reaction, a compound called an alkyl halide is reacted with magnesium metal in the presence of a solvent.
    The reaction produces a Grignard reagent, which can be further converted into 2(1H)-Pyrimidinone, 5-acetyl-4-methyl- (9CI) through a series of chemical reactions.


    1. The Reduction of a Carboxylic Acid

    2(1H)-Pyrimidinone, 5-acetyl-4-methyl- (9CI) can also be synthesized by reducing a carboxylic acid with a reducing agent such as lithium aluminum hydride (LiAlH4) or hydrogen in the presence of a catalyst such as palladium on barium sulfate.


    1. The Hydrolysis of a Nitrile

    2(1H)-Pyrimidinone, 5-acetyl-4-methyl- (9CI) can be synthesized by hydrolyzing a nitrile with a strong acid such as sulfuric acid.
    The reaction produces a compound called an amide, which can be further converted into 2(1H)-Pyrimidinone, 5-acetyl-4-methyl- (9CI) through a series of chemical reactions.


    Conclusion


    2(1H)-Pyrimidinone, 5-acetyl-4-methyl- (9CI) is an important organic compound that has numerous applications in the chemical industry.
    The synthetic routes discussed in this article are just a few of the many methods that can be used to manufacture this compound.
    The choice of synthetic route depends on various factors such as the availability of starting materials, the purity of the desired product, and the cost 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.