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    Home > Medical News > Medical World News > The Synthetic Routes of 3-chloro-4-methylpicolinonitrile

    The Synthetic Routes of 3-chloro-4-methylpicolinonitrile

    • Last Update: 2023-05-05
    • Source: Internet
    • Author: User
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    3-chloro-4-methylpicolinonitrile is a versatile organic compound that finds widespread use in various industries, including the chemical, pharmaceutical, and agrichemical industries.
    This compound is commonly used as an intermediate in the production of various chemicals, drugs, and pesticides.


    One of the most commonly used methods for the synthesis of 3-chloro-4-methylpicolinonitrile is the "nitration of 3-methylpicolinone" route.
    In this route, the nitrating agent nitrating acid is used to convert 3-methylpicolinone, a solid precursor, into 3-chloro-4-methylpicolinonitrile.
    This route is simple and straightforward, and the resulting product is of high purity.


    Another common synthetic route for 3-chloro-4-methylpicolinonitrile is the "pyrrolization of 4-chloro-3-methylpicolinone" route.
    In this route, the precursor 4-chloro-3-methylpicolinone is heated in the presence of a pyrrolyzer catalyst, such as ferric chloride, to produce 3-chloro-4-methylpicolinonitrile.
    This route is also simple and straightforward, and the resulting product is of high purity.


    In addition to the above-mentioned routes, there are several other synthetic routes for the synthesis of 3-chloro-4-methylpicolinonitrile, including the "reduction of 4-chloro-3-methylnitrobenzene" route, the "nitration of 4-chloro-3-methylaniline" route, and the "nitration of 4-chloro-3-methylaniline with hydriodic acid" route.
    These routes are all variations on the basic nitration reaction and involve the use of various reagents and catalysts to convert the precursor compounds into the desired product.


    The choice of synthetic route for the production of 3-chloro-4-methylpicolinonitrile depends on various factors, including the availability of starting materials, the desired purity of the final product, and the cost and efficiency of the synthesis.
    In general, the nitration of 3-methylpicolinone and pyrrolization of 4-chloro-3-methylpicolinone routes are the most commonly used synthetic routes for the production of this compound, due to their simplicity and high yield.


    Once synthesized, 3-chloro-4-methylpicolinonitrile is typically purified by recrystallization or by chromatography to remove any impurities.
    The purified compound is then used as an intermediate in the production of various chemicals, drugs, and pesticides.
    For example, it can be converted into caffeine, a common stimulant, through a series of chemical reactions.
    It can also be used in the production of atropine, a popular muscarinic antagonist, and scopolamine, a sedative and anticholinergic drug.


    In the agricultural industry, 3-chloro-4-methylpicolinonitrile is used as a herbicide, a fungicide, and an insecticide.
    Its effectiveness as a herbicide is due to its ability to inhibit the activity of the enzyme acetyl-CoA carboxylase, which is essential for the production of fatty acids by plants.
    In this way, the compound disrupts the plant's energy metabolism and causes it to die.
    As a fungicide


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