26820-49-5Relevant academic research and scientific papers
Kinetic and equilibrium studies of σ-adduct formation and nucleophilic substitution in the reactions of 2-chloro-3,5-dinitropyridine and 2-ethoxy-3,5-dinitropyridine with p-substituted anilines in DMSO
Asghar, Basim H.
, p. 301 - 306 (2013/05/22)
Rate and equilibrium results for the reactions of 2-chloro-3,5- dinitropyridine and 2-ethoxy-3,5-dinitropyridine with a series of p-substituted anilines in the presence of 1,4-diazabicyclo[2.2.2]octane (DABCO) were studied in DMSO. The reactions yielded 2
Solvent hydrogen bonding and structural effects on reaction of 2-chloro-3,5-dinitropyridine with para-substituted anilines in dimethylformamide/acetonitrile mixtures
Bhuvaneshwari,Elango
scheme or table, p. 1547 - 1551 (2012/04/23)
Substitution reactions of some para-substituted anilines with 2-chloro-3,5-dinitropyridine were carried out conductometrically in dimethylformamide/acetonitrile mixtures. The rate data correlate poorly with macroscopic solvent parameters while excellently
The reaction of 2-phenoxy-3,5-dinitropyridine with substituted anilines in the presence of 1,4-diazabicyclo[2.2.2]octane in dimethyl sulfoxide: Kinetic and equilibrium studies
Asghar, Basim H.
experimental part, p. 198 - 203 (2009/07/04)
The reactions of 2-phenoxy-3,5-dinitropyridine (1) with, a series of substituted anilines (4a-d) in dimethyl sulfoxide (DMSO) in the presence of 1,4-diazabicyclo[2.2.2]octane (DABCO) yield the 2-anilino derivatives without the accumulation of intermediate
Kinetics of the reaction of 2-chloro-3,5-dinitropyridine with meta- And para-substituted anilines in methanol
El Hegazy, Fatma El-Zahraa M.,Abdel Fattah, Soheir Z.,Hamed, Ezzat A.,Sharaf, Saber M.
, p. 549 - 554 (2007/10/03)
The kinetics of the reaction of 2-chloro-3,5-dinitropyridine (1) with meta- and para-substituted anilines (2a-j) to give 2-anilino-3,5-dinitropyridine derivatives (3a-j) were studied in methanol at different temperatures. IR studies of the products (3a-j)
