Rapid and scalable ruthenium catalyzed meta-C–H alkylation enabled by resonant acoustic mixing

Synthetic chemistry approaches for direct C–H bond alkylation offers a promising alternative to traditional functional-group-centered strategies which often involve multi-step procedures and may suffer from a variety of challenges including scalability. Here, we introduce resonant mixing as an effic...

Full description

Saved in:
Bibliographic Details
Published inCommunications chemistry Vol. 7; no. 1; pp. 295 - 7
Main Authors Dey, Arnab, Kancherla, Rajesh, Pal, Kuntal, Kloszewski, Nathan, Rueping, Magnus
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 18.12.2024
Nature Publishing Group
Nature Portfolio
Subjects
Online AccessGet full text
ISSN2399-3669
2399-3669
DOI10.1038/s42004-024-01390-1

Cover

More Information
Summary:Synthetic chemistry approaches for direct C–H bond alkylation offers a promising alternative to traditional functional-group-centered strategies which often involve multi-step procedures and may suffer from a variety of challenges including scalability. Here, we introduce resonant mixing as an efficient method for meta -C–H alkylation of arenes using a Ru-catalyst, avoiding the need for bulk solvents, external temperature, or light. The described methodology is highly rapid, enabling multigram-scale synthesis of meta -alkylation products within a short reaction time and achieving a very high turnover frequency. The reaction operates via a radical mechanism and is characterized by its mild reaction conditions, substrate compatibility, and exceptional meta -selectivity, all while significantly reducing reaction times. Synthetic chemistry approaches for direct C–H bond alkylation offers a promising alternative to traditional functional-group-centered strategies which often involve multi-step procedures and may suffer from a variety of challenges including scalability. Here, the authors introduce resonant acoustic mixing as an efficient method for meta -C–H alkylation of arenes using a Ru-catalyst via a radical mechanism, avoiding the need for bulk solvents, external temperature, or light.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:2399-3669
2399-3669
DOI:10.1038/s42004-024-01390-1