Journals / Turkish Journal of Chemistry / 2015 / Cilt: 39 - Sayı: 6

Synthesis, characterization, and microwave-assisted catalytic activity in Heck, Suzuki, Sonogashira, and Buchwald--Hartwig cross-coupling reactions of novel benzimidazole salts bearing N-phthalimidoethyl and benzyl moieties

Pages
1265–1278
Publication Date
2015-12-04
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The efficiency of the catalyst system in these four reactions was discussed as well as the electron-releasing and withdrawing substituent effects on the benzimidazole ligands.

📌 3 Key Takeaways

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Objective & Hypothesis:Five novel benzimidazole salts (\textbf{1}--\textbf{5}) having N-phthalimidoethyl and 4-substituted benzyl were synthesized and identified by $^{1}$H NMR, $^{13}$C NMR, and IR spectroscopic methods and microanalysis.
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Key Findings & Data:A mixture of the benzimidazole salts (\textbf{1}--\textbf{5}), Pd(OAc)$_{2}$, and K$_{2}$CO$_{3}$ in DMF-H$_{2}$O catalyzed, in high yield, the Suzuki--Miyaura and the Heck--Mizoroki cross-coupling reactions assisted by microwave irradiation in 5 min.
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Conclusion & Impact:The efficiency of the catalyst system in these four reactions was discussed as well as the electron-releasing and withdrawing substituent effects on the benzimidazole ligands.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Heck--Mizoroki coupling · Suzuki--Miyaura coupling · Sonogashira coupling

Abstract

Five novel benzimidazole salts (\textbf{1}--\textbf{5}) having N-phthalimidoethyl and 4-substituted benzyl were synthesized and identified by $^{1}$H NMR, $^{13}$C NMR, and IR spectroscopic methods and microanalysis. A mixture of the benzimidazole salts (\textbf{1}--\textbf{5}), Pd(OAc)$_{2}$, and K$_{2}$CO$_{3}$ in DMF-H$_{2}$O catalyzed, in high yield, the Suzuki--Miyaura and the Heck--Mizoroki cross-coupling reactions assisted by microwave irradiation in 5 min. The novel benzimidazole salts (\textbf{1}--\textbf{5}), Pd(OAc)$_{2}$, Cs$_{2}$CO$_{3}$, PEG, and Cu nanoparticles catalyzed, in high yield, the Sonogashira coupling reaction promoted by microwave irradiation in 10 min. The same benzimidazole salts (\textbf{1}--\textbf{5}), Pd(OAc)$_{2}$, Cs$_{2}$CO$_{3}$, and TBAB catalyzed, in moderate or low yield, the Buchwald--Hartwig reaction assisted by microwave irradiation in 60 min. The efficiency of the catalyst system in these four reactions was discussed as well as the electron-releasing and withdrawing substituent effects on the benzimidazole ligands.

Özet

Five novel benzimidazole salts (\textbf{1}--\textbf{5}) having N-phthalimidoethyl and 4-substituted benzyl were synthesized and identified by $^{1}$H NMR, $^{13}$C NMR, and IR spectroscopic methods and microanalysis. A mixture of the benzimidazole salts (\textbf{1}--\textbf{5}), Pd(OAc)$_{2}$, and K$_{2}$CO$_{3}$ in DMF-H$_{2}$O catalyzed, in high yield, the Suzuki--Miyaura and the Heck--Mizoroki cross-coupling reactions assisted by microwave irradiation in 5 min. The novel benzimidazole salts (\textbf{1}--\textbf{5}), Pd(OAc)$_{2}$, Cs$_{2}$CO$_{3}$, PEG, and Cu nanoparticles catalyzed, in high yield, the Sonogashira coupling reaction promoted by microwave irradiation in 10 min. The same benzimidazole salts (\textbf{1}--\textbf{5}), Pd(OAc)$_{2}$, Cs$_{2}$CO$_{3}$, and TBAB catalyzed, in moderate or low yield, the Buchwald--Hartwig reaction assisted by microwave irradiation in 60 min. The efficiency of the catalyst system in these four reactions was discussed as well as the electron-releasing and withdrawing substituent effects on the benzimidazole ligands.

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Cite This Article

KÜÇÜKBAY, H., YILMAZ, Ü., YAVUZ, K., BUĞDAY, N. (2015). Synthesis, characterization, and microwave-assisted catalytic activity in Heck, Suzuki, Sonogashira, and Buchwald--Hartwig cross-coupling reactions of novel benzimidazole salts bearing N-phthalimidoethyl and benzyl moieties. Turkish Journal of Chemistry, Cilt: 39 - Sayı: 6, 1265–1278. https://ajindex.com/articles/184601

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