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Palladium/1,2-bis(diphenylphosphino) ethane catalysed amination of aryl halides with aliphatic/aromatic amines

The Ullmann coupling of amines with aryl iodide and bromides has been carried out efficiently using Pd(OAc) 2/1,2-bis(diphenylphosphino) ethane [DPPE] in toluene as a solvent. The effects of various parameters such as temperature, solvent, base, catalyst loading and metal–ligand ratio on the reactio...

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Published in:Journal of molecular catalysis. A, Chemical Chemical, 2006-11, Vol.259 (1), p.46-50
Main Authors: Bhanushali, Mayur J., Nandurkar, Nitin S., Bhor, Malhari D., Bhanage, Bhalchandra M.
Format: Article
Language:English
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Summary:The Ullmann coupling of amines with aryl iodide and bromides has been carried out efficiently using Pd(OAc) 2/1,2-bis(diphenylphosphino) ethane [DPPE] in toluene as a solvent. The effects of various parameters such as temperature, solvent, base, catalyst loading and metal–ligand ratio on the reaction system were studied. The reaction is applicable to a wide variety of substituted aryl amines and alkyl amines with different steric and electronic properties. ▪ The Ullmann coupling of amines with aryl iodide and bromides has been carried out efficiently using Pd(OAc) 2/1,2-bis(diphenylphosphino) ethane [DPPE] in toluene as a solvent. The effects of various parameters such as temperature, solvent, base, catalyst loading and metal–ligand ratio on the reaction system were studied. The reaction is applicable to a wide variety of substituted aryl amines and alkyl amines with different steric and electronic properties.
ISSN:1381-1169
1873-314X
DOI:10.1016/j.molcata.2006.06.014