Microwave-Assisted Synthesis of Novel 2,4-Dihydro-5-[4-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-ones and Potentiometric Determination of Their pKa in Nonaqueous Solvents
✍ Scribed by Musa Özil; Fatih İslamoğlu; Emre Menteşe; Bahittin Kahveci
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- German
- Weight
- 231 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
The novel 4-amino-or 4-aryl-substituted 2,4-dihydro-5-[(4-trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-ones 3a -3g were synthesized by reaction of N-(ethoxycarbonyl)-4-(trifluoromethyl)benzenehydrazonic acid ethyl ester (2) and primary amines or hydrazine by microwave irradiation. Compounds 3a -3g were potentiometrically titrated with tetrabutylammonium hydroxide (Bu 4 NOH) in four nonaqueous solvents, i.e., i PrOH, t BuOH, MeCN, and N,N-dimethylformamide (DMF). Also half-neutralization potential values and the corresponding pK a values were determined in all cases.
📜 SIMILAR VOLUMES
Synthesis of 3
## Abstract 4‐Hydroxy‐2‐oxo‐2__H__‐1‐benzopyran‐3‐carboxaldehydes **2a‐d** are prepared from 4‐hydroxy‐2‐oxo‐2__H__‐1‐benzopyrans **1a‐d** __via__ the Vielsmeyer Haack reaction. The 4‐hydroxy‐2‐oxo‐3‐(3′oxo‐3′‐phenylprop‐1′‐enyl)‐2__H__‐1‐benzopyrans **3a‐d** are obtained from **2a‐d** __via__ the