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.
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