z-logo
open-access-imgOpen Access
Base- and Additive-Free Ir-Catalyzed ortho-Iodination of Benzoic Acids: Scope and Mechanistic Investigations
Author(s) -
Elis Erbing,
Amparo SanzMarco,
Ana VázquezRomero,
Jesper Malmberg,
Magnus J. Johansson,
Enrique GómezBengoa,
Belén MartínMatute
Publication year - 2017
Publication title -
acs catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.898
H-Index - 198
ISSN - 2155-5435
DOI - 10.1021/acscatal.7b02987
Subject(s) - halogenation , iridium , catalysis , chemistry , moiety , benzoic acid , combinatorial chemistry , catalytic cycle , solvent , organic chemistry , base (topology) , mathematical analysis , mathematics
A protocol for the C–H activation/iodination of benzoic acids catalyzed by a simple iridium complex has been developed. The method described in this paper allows the ortho-selective iodination of a variety of benzoic acids under extraordinarily mild conditions in the absence of any additive or base in 1,1,1,3,3,3-hexafluoroisopropanol as the solvent. The iridium catalyst used tolerates air and moisture, and selectively gives ortho-iodobenzoic acids with high conversions. Mechanistic investigations revealed that an Ir(III)/Ir(V) catalytic cycle operates, and that the unique properties of HFIP enables the C–H iodination using the carboxylic moiety as a directing group.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom