In this work, we report the unexpected conversion of a pyridine derivative into the corresponding N-benzylated pyridinium salt due to the presence of unreacted benzyl bromide in the crude product. This transformation was observed at room temperature in a solvent-free environment and without any stirring. These interesting data show how pyridinium salts can be formed in mild conditions, avoiding high temperatures that could promote the degradation of the desired product.

2-(1-Methoxycarbonyl-2-phenyleth-1-yl)-1-benzylpyridin-1-ium Bromide / L. Suigo, V. Straniero, E. Valoti. - In: MOLBANK. - ISSN 1422-8599. - 2023:4(2023 Oct 16), pp. M1738.1-M1738.5. [10.3390/M1738]

2-(1-Methoxycarbonyl-2-phenyleth-1-yl)-1-benzylpyridin-1-ium Bromide

L. Suigo
Primo
;
V. Straniero
Penultimo
;
E. Valoti
Ultimo
2023

Abstract

In this work, we report the unexpected conversion of a pyridine derivative into the corresponding N-benzylated pyridinium salt due to the presence of unreacted benzyl bromide in the crude product. This transformation was observed at room temperature in a solvent-free environment and without any stirring. These interesting data show how pyridinium salts can be formed in mild conditions, avoiding high temperatures that could promote the degradation of the desired product.
quaternary ammonium salts; α-carbon benzylation; N-benzylation;
Settore CHIM/06 - Chimica Organica
Settore CHIM/08 - Chimica Farmaceutica
16-ott-2023
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1009850
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