Title of article
Novel quinoline–imidazolium adducts via the reaction of 2-oxoquinoline-3-carbaldehyde and quinoline-3-carbaldehydes with 1-butyl-3-methylimidazolium chloride [BMIM][Cl]
Author/Authors
Laali، نويسنده , , Kenneth K. and Insuasty، نويسنده , , Daniel and Abonia، نويسنده , , Rodrigo and Insuasty، نويسنده , , Braulio and Bunge، نويسنده , , Scott D.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2014
Pages
5
From page
4395
To page
4399
Abstract
A library of hydroxyquinolin-3-ylmethylimidazolium adducts were prepared in high yields from the reaction of [BMIM][Cl] with various substituted quinoline-3-carbaldehydes and 2-oxoquinoline-3-carbaldehydes under mild conditions by using sodium acetate in MeCN under ultrasound irradiation. The use of sodium acetate and imidazolium chloride was crucial for the success of these CC bond forming reactions. Attempted coupling with thiazolium bromide led instead to quinoline-3-carboxylic acid.
Keywords
Quinolone-3-carbaldehyde , Ionic liquids (IL’s) , 3-Butyl-1-methylimidazolium acetate , Hydroxyquinolin-3-ylmethylimidazolium adducts , N-Heterocyclic carbenes (NHCs) , thiazolium salts
Journal title
Tetrahedron Letters
Serial Year
2014
Journal title
Tetrahedron Letters
Record number
1890297
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