Electrooxidative C–H/O–H bond coupling via Ru catalysis: access to phthalides and naphtho[1,8-bc]furans

Abstract

We hereby report ruthenium-catalyzed electrooxidative coupling of acrylates with benzoic acids and naphthol for the synthesis of phthalide and naphthofuran derivatives. The process is particularly effective for activating weakly coordinating O–H bonds using ruthenium catalysts. This method is workable and well-organized for the activation of carbon–hydrogen and oxygen–hydrogen bonds, demonstrating moderate to good yields across a diverse set of over 26 readily available substrates. The method proceeds under oxidant- and additive-free conditions, significantly reducing the reaction time while retaining a broad substrate scope. Our approach provides a green and user-friendly method for synthesizing phthalides and naphthofurans via weak coordination O–H and C–H bond activation, leveraging electricity as an oxidant.

Graphical abstract: Electrooxidative C–H/O–H bond coupling via Ru catalysis: access to phthalides and naphtho[1,8-bc]furans

Supplementary files

Transparent peer review

To support increased transparency, we offer authors the option to publish the peer review history alongside their article.

View this article’s peer review history

Article information

Article type
Paper
Submitted
13 Kho 2025
Accepted
02 Maw 2025
First published
02 Maw 2025

Catal. Sci. Technol., 2025, Advance Article

Electrooxidative C–H/O–H bond coupling via Ru catalysis: access to phthalides and naphtho[1,8-bc]furans

N. Patil, A. Dhapate, T. Bharadwaj and B. M. Bhanage, Catal. Sci. Technol., 2025, Advance Article , DOI: 10.1039/D5CY00713E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements