Palladium-Catalyzed Ortho-Selective C–H Oxidative Carbonylation of N-Substituted Anilines with CO and Primary Amines for the Synthesis of o-Aminobenzamides
Abstract:An efficient, one-pot strategy with high selectivity and high atom economy for the synthesis of o-aminobenzamides has been developed via palladium-catalyzed ortho-selective C-H oxidative carbonylation of N-substituted anilines with CO and primary amines. A wide range of N-substituted anilines and primary amines can be tolerated in this transformation to afford the corresponding o-aminobenzamides in moderate to excellent yields under mild conditions.
“…In 2016, the group of Zhang reported a practical intermolecular aminocarbonylation of anilines for the construction of o-aminobenzamides (Scheme 21). 29 The employment of C-H activation for aminocarbonylation with CO as C1 source is an elegant solution for the synthesis of amides. In this work, both aromatic and aliphatic primary amines were utilized as the coupling partners.…”
Carbon monoxide, which is an abundant and inexpensive carbonyl source, has been widely applied to synthesize carbonyl-containing compounds, for example ketones, esters, and amides.
“…In 2016, the group of Zhang reported a practical intermolecular aminocarbonylation of anilines for the construction of o-aminobenzamides (Scheme 21). 29 The employment of C-H activation for aminocarbonylation with CO as C1 source is an elegant solution for the synthesis of amides. In this work, both aromatic and aliphatic primary amines were utilized as the coupling partners.…”
Carbon monoxide, which is an abundant and inexpensive carbonyl source, has been widely applied to synthesize carbonyl-containing compounds, for example ketones, esters, and amides.
“…In 2016, Zhang and co-workers developed an efficient palladium-catalyzed directed oxidative intermolecular C-H aminocarbonylation of N-alkylanilines with Cu(OAc) 2 and O 2 as the oxidants (Scheme 2a). 21 The reaction exhibits excellent ortho-selectivity and monocarbonylation, affording various ortho-aminobenzamides in good yields from primary amines. The ortho-selectivity might result from the formation of an ortho-aminoaryl-palladium dimer intermediate.…”
The amide linkage is one of the most important structural moieties in both chemistry and biology. Here, we briefly discuss recent advances in catalytic intermolecular C–H carbonylation reactions for the synthesis of amides, with particular attention to our intermolecular C–H amidation of arenes with carbon monoxide and organic azides to produce amides.1 Introduction2 Representative Methods for Amide Synthesis3 C–H Aminocarbonylation with Carbon Monoxide and Amines4 C–H Amidation to Amides with Carbon Monoxide and Azides5 Summary and Outlook
“…Nowadays, directing‐group‐assisted carbonylation of simple C–H bonds has emerged as an ideal strategy, through the introduction of carbon monoxide, to construct a variety of carbonyl compounds. Numerous directing groups such as amides, amines, heteroatoms and hydroxy groups have been used for C–H bond carbonylation . However, most progress has been achieved with compounds containing directing groups and with the use of hazardous metals and oxidants such as copper, silver salts or peroxides, which are undesirable from a green chemistry point of view.…”
This work reports the synthesis of p‐hydroxybenzoates directly from phenols by oxidative carbonylation of phenolic C–H bonds, proceding through oxidative iodination. The developed methodology is efficient and economically attractive because phenols are cheap and easily available starting materials. This one‐pot strategy was expediently applied to the synthesis of a variety of p‐hydroxybenzoates by utilizing simple primary and secondary alcohols with different phenols under mild reaction conditions. Advantageously, the procedure has no need for co‐catalysts, co‐solvents or external ligands. The utilization of molecular oxygen as a terminal oxidant for C–H bond oxidation represents an additional benefit.
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