Ultrasound Promoted Simple and Efficient N-Alkylation of 2-Substituted Benzimidazoles
Corresponding Author(s) : P.N. Kishore Babu
kishore1136@gmail.com
Asian Journal of Chemistry,
Vol. 24 No. 12 (2012): Vol 24 Issue 12
Abstract
N-Alkylation of 2-chlorobenzimidazole was carried out using different alkylating agents under ultrasound irradiation technique. These reactions were completed in shorter times and with higher percentage of yields. Among all the green solvents, triethanolamine was found to be very effective and also acts as a base. The above reaction conditions were extended to other 2-substituted benzimidazoles. Thus, a simple and efficient route for N-alkylation has been developed using ultrasound irradiation technique.
Keywords
Ultrasonic waves
PEG-600
Triethanolamine
N-alkylations
Kishore Babu, P., Rama Devi, B., & Dubey, P. (2012). Ultrasound Promoted Simple and Efficient N-Alkylation of 2-Substituted Benzimidazoles. Asian Journal of Chemistry, 24(12), 5756–5758. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/9981
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