Efficient Ibuprofen synthesis from isobutyl-benzene under ambient conditions

Ibuprofen is classified as a non-steroidal anti-inflammatory medication (NSAID). This medication is employed for the treatment of several ailments, encompassing mild to moderate pain such as toothache, migraine, and period pain. Additionally, it is used to alleviate high-temperature fevers resembling influenza, reduce inflammation in tissues, and manage conditions like rheumatoid arthritis, back pain, and gout, among others. Despite the relative simplicity of ibuprofen's structure, it possesses significant structural complexity to enable a broader variety of acquisition methods. Numerous techniques for acquiring it with possible industrial utility have been discovered since the inception of its initial commercial use. The majority of commercially viable industrial processes utilized for the synthesis of ibuprofen are derived from isobutyl-benzene (IBB). Commercial isobutyl benzene (IBB) is synthesized through the reaction between propene and toluene. The conversion of isobutyl benzene ranges from (18.05%) to (19.8%) at various values of reaction temperature and from the results we can see that the reaction time has a significant effect on the isobutyl benzene conversion.