echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Drugs Articles > The Synthetic Routes of (R)-(+)-2-(DIPHENYLMETHYL)PYRROLIDINE

    The Synthetic Routes of (R)-(+)-2-(DIPHENYLMETHYL)PYRROLIDINE

    • Last Update: 2023-05-11
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    (R)-(+)-2-(Diphenylmethyl)pyrrolidine is a synthetic compound that has various applications in the chemical industry.
    It is an important intermediate in the production of several pharmaceuticals, agrochemicals, and specialty chemicals.
    The compound can be synthesized through several methods, and in this article, we will discuss some of the most commonly used synthetic routes for (R)-(+)-2-(Diphenylmethyl)pyrrolidine.


    One of the most straightforward methods for synthesizing (R)-(+)-2-(Diphenylmethyl)pyrrolidine is through a condensation reaction between phenyl acetate and proline.
    The reaction is carried out in the presence of a solvent such as methanol or ethanol, and the product is isolated by filtration or recrystallization.
    This method is simple and relatively inexpensive, making it a popular choice for industrial-scale synthesis.


    Another synthetic route for (R)-(+)-2-(Diphenylmethyl)pyrrolidine involves a sequence of reactions starting with the synthesis of the amino acid, β-alanine.
    This is followed by a reaction with chloroformic acid, which converts the amino acid into a chloride salt.
    The salt is then hydrolyzed using a strong acid such as hydrochloric acid to form the free base, (R)-(+)-2-(Diphenylmethyl)pyrrolidine.
    The product is then isolated by filtration or recrystallization.


    A more recent synthetic route for (R)-(+)-2-(Diphenylmethyl)pyrrolidine involves the use of a metal catalyst, such as racemic RuCl2.
    H2O, in a hydrogenation reaction of a precursor such as N-phenylpropionamide.
    The reaction is carried out in the presence of a solvent such as THF or DME and the product is isolated by filtration or recrystallization.
    This method is more efficient and selective compared to the traditional methods and is becoming increasingly popular in industry.


    (R)-(+)-2-(Diphenylmethyl)pyrrolidine can also be synthesized through a sequence of reactions starting with the reduction of benzyl bromide using lithium aluminum hydride (LAH).
    This is followed by a reaction with 3-nitro-l-phenylalanine to form a mixed anhydride, which is then reduced using LAH.
    The product is then extracted with a solvent such as ether and dried over anhydrous sodium sulfate.
    The product is then isolated by filtration or recrystallization.


    In conclusion, (R)-(+)-2-(Diphenylmethyl)pyrrolidine is a versatile compound with several synthetic routes available in the chemical industry.
    The choice of synthetic route depends on factors such as cost, efficiency, and selectivity, and it is important for chemical engineers and technicians to understand the various options available to them when synthesizing this compound.


    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.