scholarly journals Benzylation of N-phenyl-2-phenylacetamide under microwave irradiation

2008 ◽  
Vol 73 (10) ◽  
pp. 945-950 ◽  
Author(s):  
Dusan Mijin ◽  
Masa Prascevic ◽  
Slobodan Petrovic

N-Phenyl-2-phenylacetamide was alkylated with benzyl chloride in the presence of powdered potassium hydroxide under microwave irradiation in a solvent-free system. The reactions were also performed in the presence of phase-transfer catalysts. The formation of N-, O- and C-products of alkylation was followed by gas chromatography. The N-product was found to be the main product under microwave irradiation. The O-product was obtained in higher yields when an excess of base and benzyl chloride was used.

2004 ◽  
Vol 69 (2) ◽  
pp. 85-92 ◽  
Author(s):  
Dusan Mijin ◽  
Vida Jankovic ◽  
Slobodan Petrovic

Benzylation of N-(4-chlorophenyl)-2-phenylacetamidewith benzyl chloride in the presence of powdered potassium hydroxide under various reaction conditions was performed in order to establish the possible reaction products. Different temperatures and ratios of reactants and solvents were used. The reactions were also carried out in the presence of different phase-transfer catalysts in toluene as a solvent. The formation of the reaction products was followed using gas chromatography. On the basis of the obtained results, the reactivity and the orientation in the alkylation reaction of the investigated amide is discussed.


2016 ◽  
Vol 93 (10) ◽  
pp. 1399-1406 ◽  
Author(s):  
Andressa C. H. Weber ◽  
Thaís C. Batista ◽  
Bruno Gonçalves ◽  
Carolina R. L. Hack ◽  
Larissa M. Porciuncula ◽  
...  

2002 ◽  
Vol 67 (6) ◽  
pp. 373-379 ◽  
Author(s):  
Vida Jankovic ◽  
Dusan Mijin ◽  
Slobodan Petrovic

N-(4-Nitrophenyl)-2-phenylacetamide was alkylated with benzyl chloride in the presence of powdered potassium hydroxide at different temperatures and in various solvents in order to establish the reactivity and orientation in the reaction. The reactions were also carried out in the presence of different phase-transfer catalysts in toluene. Product formation was followed by GC. The obtained results were compared to the results of the benzylation of other N-substituted 2-phenylacetamides, especially of N-phenyl-2-phenylacetamide.


Tetrahedron ◽  
2009 ◽  
Vol 65 (50) ◽  
pp. 10370-10376 ◽  
Author(s):  
Marc Escribà ◽  
Jordi Eras ◽  
Miquel Duran ◽  
Sílvia Simon ◽  
Cristina Butchosa ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document