Synthesis of α/β-Aromatic Peroxy Thiols Mediated by Iodine Source
Kaifa Zhang1, Changhong Liu1, Dilshat Abdukerem1
1State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources; Urumqi Key Laboratory of Green and Synthesis Technology Key Laboratory of Oil and Fine Chemicals; College of Chemistry, Xinjiang University, Urumqi 830017, China.
Abstract:
Peroxygenated compounds have wide applications in various fields, including chemistry, pharmaceutical chemistry, medicine, and materials science. However, there is still a need for more efficient and environmentally friendly synthesis methods for such compounds. Herein, we investigated the two-step, one-pot, regioselective synthesis of α/β-aromatic peroxy thiols. We explored various substrates and solvents for the reaction and identified the optimal reaction conditions. We successfully obtained several peroxy thiols in moderate to good yields via the selective generation of effective intermediates of iodoalkyl peroxides at room temperature without the need for metal catalysts.
More Related Videos
10:14Synthesis and Purification of Iodoaziridines Involving Quantitative Selection of the Optimal Stationary Phase for Chromatography
Published on: May 16, 2014
08:47Synthesis and Bioconjugation of Thiol-Reactive Reagents for the Creation of Site-Selectively Modified Immunoconjugates
Published on: March 6, 2019
Related Concept Videos
Preparation and Reactions of Thiols
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Preparation and Reactions of Sulfides
Radical Substitution: Allylic Bromination
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
