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Ultrason Sonochem ; 16(6): 711-7, 2009 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-19442560

RESUMO

A mild, efficient, facile and eco-friendly procedure for the synthesis of 2,4-diarylthiazoles from arylthioamides and alpha-bromoacetophenones in 1-n-butyl-3-methylimidazolium tetrafluoroborate as a "green" media under ultrasound irradiation at room temperature is described. It is interesting to mention that only one product was obtained when two different alpha-bromoacetophenones were reacted with 1,3-phenyl dithioamide as the substrate. Work-up is very simple and there is no need to purify the product. A recycling study confirmed that the ionic liquid can be reused multiple times without a significant loss in its activity.


Assuntos
Química Verde/métodos , Imidazóis/química , Temperatura , Tiazóis/síntese química , Ultrassom , Solventes/química , Tiazóis/química
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