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Medientyp: E-Artikel Titel: Ultrasound‐Promoted Reaction of 2‐Chlorobenzoic Acids and Aliphatic Amines Beteiligte: Docampo, Maite L.; Pellón, Rolando F.; Estevez‐Braun, Ana; Ravelo, Angel G. Erschienen: Wiley, 2007 Erschienen in: European Journal of Organic Chemistry, 2007 (2007) 24, Seite 4111-4115 Sprache: Englisch DOI: 10.1002/ejoc.200700281 ISSN: 1434-193X; 1099-0690 Schlagwörter: Organic Chemistry ; Physical and Theoretical Chemistry Entstehung: Anmerkungen: Beschreibung: <jats:title>Abstract</jats:title><jats:p>An improvement to the use of DMF as a solvent for the condensation of 2‐chlorobenzoic acids with aliphatic primary or secondary amines was described. A number of alkylaminobenzoic acids and dialkylaminobenzoic acids were synthesized in acceptable‐to‐good yield. The advantages of this procedure include readily available substrates, the use of an inexpensive copper powder without taking any precautions to exclude moisture under mild conditions and experimental ease. Furthermore, this condensation could also be achieved under nonclassical conditions by using ultrasonic irradiation at room temperature. We demonstrated that ultrasound‐promoted condensation of 2‐chlorobenzoic acid with aliphatic amines with the use of DMF as the solvent, especially in the case of secondary amines, affords products in high yields and reduces the reaction time to minutes. The results proved to be highly reproducible because the relevant sonochemical parameters were rigorously controlled.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)</jats:p>