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Alkylation of N-ethyl-2-phenylacetamide with benzyl halides

dc.creatorMijin, Dušan
dc.creatorBožić, Biljana M.
dc.creatorStojanović, N.D.
dc.creatorPetrović, Slobodan
dc.date.accessioned2021-03-10T09:37:17Z
dc.date.available2021-03-10T09:37:17Z
dc.date.issued1996
dc.identifier.issn0352-5139
dc.identifier.urihttp://TechnoRep.tmf.bg.ac.rs/handle/123456789/72
dc.description.abstractAlkylations of N-ethyl-2-phenylacetamide with benzyl halides (chloride, bromide and iodide) in the presence of powdered KOH were carried out in order to establish the possible reaction products as well as to ascertain optimal reaction conditions for the synthesis of different products. Reactions were carried out in the presence of different phase-transfer catalysts, solvents and temperatures. N-, O-, C-and C,N-products of alkylation were established. Non-polar solvents were found to be the best for this type of reaction.en
dc.publisherSerbian Chemical Society, Belgrade
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceJournal of the Serbian Chemical Society
dc.subjectAlkylationen
dc.subjectC,N-alkylationen
dc.subjectC-alkylationen
dc.subjectMono-N-substituted phenylacetamidesen
dc.subjectN-alkylationen
dc.subjectPhase-transfer catalysisen
dc.subjectPhenylacetamidesen
dc.titleAlkylation of N-ethyl-2-phenylacetamide with benzyl halidesen
dc.typearticle
dc.rights.licenseBY-NC-ND
dc.citation.epage1144
dc.citation.issue12
dc.citation.other61(12): 1137-1144
dc.citation.spage1137
dc.citation.volume61
dc.identifier.pmid
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_technorep_72
dc.identifier.scopus2-s2.0-0039466280
dc.type.versionpublishedVersion


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