The chemodivergent property of dimethyl sulfoxide (DMSO) along with 1,2-dichloroethane (DCE) was exploited for the incorporation of a methylene group to form diarylmethanes through a dearomatization/rearomatization process. Methyl(methylene)sulfonium ions (CH=S-Me) were generated by simple heating of commonly used solvents such as DMSO and DCE. These ions were subsequently trapped by electron-rich arenes and heteroarenes, resulting in the synthesis of both symmetrical and unsymmetrical diarylmethanes. This protocol was further extended to access -methylenamides by reacting 2-naphthol with amides or nitriles in the presence of DMSO and DCE.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.joc.3c02612DOI Listing

Publication Analysis

Top Keywords

electron-rich arenes
8
dmso dce
8
dmso-dce triggered
4
triggered chemodivergent
4
chemodivergent c-methylenation
4
c-methylenation electron-rich
4
arenes easy
4
easy access
4
access diarylmethanes
4
diarylmethanes chemodivergent
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!