Kinetics and reactivity of substituted anilines with 2??chloro??5??nitropyridine in dimethyl sulfoxide and dimethyl formamide

…, GM El??Subruiti, FEZM El??Hegazy…

Index: El-Bardan, Ali A.; El-Subruiti, Gehan M.; El-Hegazy, Fatma El-Zahraa M.; Hamed, Ezzat A. International Journal of Chemical Kinetics, 2002 , vol. 34, # 11 p. 645 - 650

Full Text: HTML

Citation Number: 17

Abstract

Abstract The kinetics of the reaction of substituted anilines with 2-chloro-5-nitropyridine were studied in dimethyl sulfonide (DMSO) and dimethyl formamide (DMF) at different amine concentrations and temperatures in the range 45–60 C. In both solvents the reaction was not a base-catalyzed one. A plot of ΔH# versus ΔS# for the reaction in DMSO and DMF gave good straight lines with isokinetic temperatures 128 C and 105 C, respectively. Good ...

Related Articles:

Palladium (II)-Catalyzed, Heteroatom-Directed, Regioselective C–H Nitration of Anilines Using Pyrimidine as a Removable Directing Group

[Chu, Jean-Ho; Huang, Hao-Ping; Hsu, Wen-Ting; Chen, Shih-Tien; Wu, Ming-Jung Organometallics, 2014 , vol. 33, # 5 p. 1190 - 1204]

Oxidative arylamination of 1, 3-dinitrobenzene and 3-nitropyridine under anaerobic conditions: The dual role of the nitroarenes

[Gulevskaya, Anna V.; Tyaglivaya, Inna N.; Verbeeck, Stefan; Maes, Bert U.W.; Tkachuk, Anna V. Arkivoc, 2011 , vol. 2011, # 9 p. 238 - 251]

More Articles...