Generic placeholder image

Letters in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

Research Article

K2PdCl4/PPh3-catalyzed Carbon-sulfur Coupling Reaction; An Efficient and One-pot Method to Direct Synthesis of Organic Disulfides/Sulfides from Aryl Halides and Thiourea

Author(s): Masoumeh Raeisi, Fariba Mohammadi, Mohammad Soleiman-Beigi* and Ali Naghipour

Volume 15 , Issue 11 , 2018

Page: [899 - 904] Pages: 6

DOI: 10.2174/1570178615666180412122502

Price: $65

Abstract

This work describes an efficient and new catalyst for the one-pot synthesis of organic disulfides/ sulfides via a palladium catalyst in the presence of PPh3 ligands for domino cross-coupling reaction of aryl halides and thiourea and then sulfur-transformation. Finally, the generated aryl thiolate converts to disulfide at normal oxidative and atmospheric conditions in DMF/water. However, thiols convert to unsymmetrical sulfides by one-pot reaction with alkyl halides in PEG/H2O.

Keywords: Palladium catalyst, organic disulfides/sulfides, cross-coupling reaction, thiourea, K2PdCl4, halides.

Graphical Abstract

Rights & Permissions Print Export Cite as
© 2022 Bentham Science Publishers | Privacy Policy