Issue 7, 2019

Iron-catalyzed protodehalogenation of alkyl and aryl halides using hydrosilanes

Abstract

A simple and efficient iron-catalyzed protodehalogenation of alkyl and aryl halides using phenylhydrosilane is disclosed. The reaction utilizes FeCl3 without the requirement of ligands. Unactivated alkyl and aryl halides were successfully reduced in good yields; sterically hindered tertiary halides were also reduced including the less reactive chlorides. The scalability of this methodology was demonstrated by a gram-scale synthesis with a catalyst loading as low as 0.5 mol%. Notably, disproportionation of phenylsilane leads to diphenylsilane that further reduces the halides. Preliminary mechanistic studies revealed a non-radical pathway and the source of hydrogen is PhSiH3via deuterium labeling studies. Our methodology represents simplicity and provides a good alternative to typical tin, aluminum and boron hydride reagents.

Graphical abstract: Iron-catalyzed protodehalogenation of alkyl and aryl halides using hydrosilanes

Supplementary files

Article information

Article type
Communication
Submitted
23 Way 2018
Accepted
01 Xim 2018
First published
02 Xim 2018

Org. Biomol. Chem., 2019,17, 1749-1753

Iron-catalyzed protodehalogenation of alkyl and aryl halides using hydrosilanes

R. Pilli, V. Balakrishnan, R. Chandrasekaran and R. Rasappan, Org. Biomol. Chem., 2019, 17, 1749 DOI: 10.1039/C8OB02365D

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