Aminocarbonylation of aryl iodides with primary and secondary amines in aqueous medium using polymer supported palladium-N-heterocyclic carbene complex as an efficient and heterogeneous recyclable catalyst

An efficient phosphine-free protocol for the aminocarbonylation of aryl iodides with primary and secondary amines using PS-Pd-NHC complex as a heterogeneous and recyclable catalyst has been developed. The developed protocol is more advantageous due to use of water as environmentally benign solvent a...

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Published inCatalysis today Vol. 198; no. 1; pp. 148 - 153
Main Authors Qureshi, Ziyauddin S., Revankar, Santosh A., Khedkar, Mayur V., Bhanage, Bhalchandra M.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 30.12.2012
Elsevier
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Abstract An efficient phosphine-free protocol for the aminocarbonylation of aryl iodides with primary and secondary amines using PS-Pd-NHC complex as a heterogeneous and recyclable catalyst has been developed. The developed protocol is more advantageous due to use of water as environmentally benign solvent and effective catalyst recyclability. [Display omitted] ► A highly efficient phosphine free PS-Pd-NHC catalytic system for aminocarbonylation reaction of aryl iodides with primary and secondary amines was developed in aqueous medium. ► General applicability of the developed protocol was investigated. ► The developed protocol is advantageous due to use of water as environmentally benign solvent. ► The catalyst exhibited remarkable recyclability for four consecutive cycles. Aminocarbonylation of aryl iodides with primary and secondary aromatic/aliphatic amines to corresponding amides using polymer supported palladium-N-heterocyclic carbene complex (PS-Pd-NHC) as an efficient heterogeneous, recyclable catalyst is described. The catalytic system was optimized with respect to various reaction parameters to give excellent yield of desired products. The catalyst can be easily separated by simple filtration process and recycled further up to four consecutive recycle without loss in any activity and selectivity. The protocol is advantageous due to the ease in handling of the catalyst, simple workup procedure, and environmentally benign water as solvent and effective catalyst recyclability.
AbstractList An efficient phosphine-free protocol for the aminocarbonylation of aryl iodides with primary and secondary amines using PS-Pd-NHC complex as a heterogeneous and recyclable catalyst has been developed. The developed protocol is more advantageous due to use of water as environmentally benign solvent and effective catalyst recyclability. [Display omitted] ► A highly efficient phosphine free PS-Pd-NHC catalytic system for aminocarbonylation reaction of aryl iodides with primary and secondary amines was developed in aqueous medium. ► General applicability of the developed protocol was investigated. ► The developed protocol is advantageous due to use of water as environmentally benign solvent. ► The catalyst exhibited remarkable recyclability for four consecutive cycles. Aminocarbonylation of aryl iodides with primary and secondary aromatic/aliphatic amines to corresponding amides using polymer supported palladium-N-heterocyclic carbene complex (PS-Pd-NHC) as an efficient heterogeneous, recyclable catalyst is described. The catalytic system was optimized with respect to various reaction parameters to give excellent yield of desired products. The catalyst can be easily separated by simple filtration process and recycled further up to four consecutive recycle without loss in any activity and selectivity. The protocol is advantageous due to the ease in handling of the catalyst, simple workup procedure, and environmentally benign water as solvent and effective catalyst recyclability.
Aminocarbonylation of aryl iodides with primary and secondary aromatic/aliphatic amines to corresponding amides using polymer supported palladium-N-heterocyclic carbene complex (PS-Pd-NHC) as an efficient heterogeneous, recyclable catalyst is described. The catalytic system was optimized with respect to various reaction parameters to give excellent yield of desired products. The catalyst can be easily separated by simple filtration process and recycled further up to four consecutive recycle without loss in any activity and selectivity. The protocol is advantageous due to the ease in handling of the catalyst, simple workup procedure, and environmentally benign water as solvent and effective catalyst recyclability.
Author Bhanage, Bhalchandra M.
Khedkar, Mayur V.
Revankar, Santosh A.
Qureshi, Ziyauddin S.
Author_xml – sequence: 1
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  fullname: Revankar, Santosh A.
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  givenname: Mayur V.
  surname: Khedkar
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  givenname: Bhalchandra M.
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  email: bm.bhanage@ictmumbai.edu.in, bm.bhanage@gmail.com
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Issue 1
Keywords Heterogeneous catalysis
Palladium
Aryl iodides
Primary–secondary amine
Aminocarbonylation
Water
Catalytic reaction
Filtration
Iodides
Support
Recyclable catalyst
Polymer
Transition metal
Selectivity
Carbene
Primary-secondary amine
Aqueous medium
Aryl
Primary amine
Platinoid
Secondary amine
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Snippet An efficient phosphine-free protocol for the aminocarbonylation of aryl iodides with primary and secondary amines using PS-Pd-NHC complex as a heterogeneous...
Aminocarbonylation of aryl iodides with primary and secondary aromatic/aliphatic amines to corresponding amides using polymer supported...
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SubjectTerms amides
Aminocarbonylation
Aryl iodides
Catalysis
catalytic activity
Chemistry
Exact sciences and technology
filtration
General and physical chemistry
Heterogeneous catalysis
iodides
Palladium
polymers
Primary–secondary amine
secondary amines
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
Title Aminocarbonylation of aryl iodides with primary and secondary amines in aqueous medium using polymer supported palladium-N-heterocyclic carbene complex as an efficient and heterogeneous recyclable catalyst
URI https://dx.doi.org/10.1016/j.cattod.2012.03.039
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