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dc.contributor.authorBradley, Lynn M.
dc.contributor.authorDemas, Maria
dc.date.accessioned2018-04-07T16:03:48Z
dc.date.available2018-04-07T16:03:48Z
dc.date.issued1998
dc.identifier.citationBradley, L.M.; Hunt, D.A. “Metalation Reactions of 3,5-Dichloro-N,N-diethylbenzamide,” The College of New Jersey Journal of Student Scholarship, April 1998.en_US
dc.identifier.urihttp://www.tcnj.edu/documents-large/joss/1998.pdf
dc.description.abstractThe competing influences of regiocontrol of the diethylamido and chloro functional groups were examined in the metalation reactions of 3,5-dichloro-N,N-diethylbenzamide. The compounds, 3,5-dichloro-4-methyl-N,Ndiethylbenzamide and 2,6-dichloro-4-N,Ndiethylamide benzoic acid, were synthesized by reacting 3,5 -dichloro-N,N -diethy lbenzamide with butyllithium (BuLi) followed by iodomethane (CH3I) and carbon dioxide (C02), respectively. The observed site of metalation was controlled by the chlorine substituents, rather than the amide substituent. The products were characterized using silicagel TLC, Varian Gemini 300MHz 1H-NMR spectroscopy, and mass spectroscopy (MS).en_US
dc.description.sponsorshipCollege of New Jersey (Ewing, N.J.). Office of Academic Affairs
dc.language.isoen_USen_US
dc.publisherThe College of New Jerseyen_US
dc.titleMetalation Reactions of 3,5-Dichloro-N,N-diethylbenzamideen_US
dc.typeArticleen_US
dc.typeTexten_US
prism.publicationNameThe College of New Jersey Journal of Student Scholarship
prism.volume1
prism.publicationDate1998
prism.startingPage8
prism.endingPage13
dc.identifier.handlehttps://dr.tcnj.edu/handle/2900/2233


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