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Lee, Jae Sung
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STOICHIOMETRY OF PALLADIUM-CATALYZED N,N'-DIPHENYLUREA SYNTHESIS FROM NITROBENZENE, ANILINE AND CARBON-MONOXIDE

Alternative Title
STOICHIOMETRY OF PALLADIUM-CATALYZED N,N'-DIPHENYLUREA SYNTHESIS FROM NITROBENZENE, ANILINE AND CARBON-MONOXIDE
Author(s)
LEE, Sang MooCHO, Nag SugKIM, Kye DuckOH, Jae SeungLEE, Chul WooLee, Jae Sung
Issued Date
1992-04
DOI
10.1016/0304-5102(92)80060-T
URI
https://scholarworks.unist.ac.kr/handle/201301/13023
Fulltext
http://www.sciencedirect.com/science/article/pii/030451029280060T#
Citation
JOURNAL OF MOLECULAR CATALYSIS, v.73, no.1, pp.43 - 49
Abstract
By using deuterated nitrobenzene as a reactant, it was found that Pd-catalyzed synthesis of N,N'-diphenylurea from nitrobenzene, aniline and CO proceeded via two parallel routes: (i) PhNO2+PhNH2+3CO-->PhNHCONHPh+2CO2, and (ii) PhNO2+5PhNH2+3CO -->3PhNHCONHPh+2H2O. The relative importance of these two routes depended strongly on the ratio of aniline to nitrobenzene initially fed to the reactor. Mechanisms are proposed that account for these reaction stoichiometries
Publisher
Elsevier BV
ISSN
0304-5102

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