About the journal

Cobiss

Journal of the Serbian Chemical Society 2008 Volume 73, Issue 10, Pages: 945-950
https://doi.org/10.2298/JSC0810945M
Full text ( 350 KB)
Cited by


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

Mijin Dušan Ž. ORCID iD icon (Katedra za organsku hemiju, Tehnološko-metalurški fakultet, Beograd)
Praščević Maša (Katedra za organsku hemiju, Tehnološko-metalurški fakultet, Beograd)
Petrović Slobodan D. (Katedra za organsku hemiju, Tehnološko-metalurški fakultet, Beograd + Hemofarm, Vršac)

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.

Keywords: alkylation, amides, phenylacetamides, phase-transfer conditions, microwave irradiation