5397-16-0Relevant articles and documents
Visible-Light-Mediated Synthesis of Amides from Aldehydes and Amines via in Situ Acid Chloride Formation
Iqbal, Naeem,Cho, Eun Jin
, p. 1905 - 1911 (2016/03/15)
An efficient visible-light photocatalysis-based one-pot amide synthesis method was developed; visible-light irradiation of a mixture of an aldehyde, tert-butyl hydrogen peroxide, and N-chlorosuccinimide using a Ru(bpy)3Cl2 photocatalyst afforded an acid chloride, which subsequently reacted with amine to yield the corresponding amide. The reaction was used to synthesize moclobemide and a D3 receptor intermediate.
Oxidation of N-benzylaldimines to N-benzylamides by MCPBA and BF3·OEt2
An, Gwang-Il,Rhee, Hakjune
, p. 876 - 878 (2007/10/03)
N-Benzylamides were obtained from the corresponding N-benzylaldimines in high yields. N-Benzylaldimines are readily prepared from the corresponding aldehydes with benzylamine. This procedure involves the oxidation of N-benzylaldimines with MCPBA with BF3·OEt2. In this reaction, the reaction presumably follows an internal hydrogen abstraction to provide only N-benzylamide.
O,O-Diethyldithiophosphoric acid. A new condensing agent for acylation of amines by carboxylic acid
Hossain,Borthakur
, p. 1062 - 1063 (2007/10/02)
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