## Abstract 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 intermediates. The kinetics is compat
Kinetics and reactivity of substituted anilines with 2-chloro-5-nitropyridine in dimethyl sulfoxide and dimethyl formamide
✍ Scribed by Ali A. El-Bardan; Gehan M. El-Subruiti; Fatma El-Zahraa M. El-Hegazy; Ezzat A. Hamed
- Book ID
- 102443189
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 87 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
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 Δ__H__^#^ versus Δ__S__^#^ for the reaction in DMSO and DMF gave good straight lines with isokinetic temperatures 128°C and 105°C, respectively. Good linear relationships were obtained from the plots of log k~1~ against σ° values at all temperatures with negative ρ values (−1.63 to −1.28 in DMSO) and (−1.26 to −0.90 in DMF). © 2002 Wiley Periodicals, Inc. Int J Chem Kinet 34: 645–650, 2002
📜 SIMILAR VOLUMES
The kinetics of the reaction of 2-chloro-3-nitropyridine (ortho-like) and 2-chloro-5-nitropyridine (para-like) with a series of aryloxide ions were studied in methanol at different temperatures. Plots of DH ≠ versus DS ≠ for both reactions gave good straight lines with isokinetic temperatures of 168