Synthesis of the symmetrical methylene diesters from carboxylic ionic liquids

D. Gómora-Herrera, I. V. Lijanova, O. Olivares-Xometl, A. Toscano, N. V. Likhanova

Research output: Contribution to journalArticle

1 Scopus citations

Abstract

© 2017 Published by NRC Research Press. The reaction between carboxylic ionic liquids and dichloromethane, which provokes the formation of symmetrical methylene diesters, was carried out. The synthesis of these ionic liquid compounds was carried out in a microwave reactor, and the characterization by spectroscopic techniques of methylene diesters (methylene di-2-furoate, methylene di-2-picolinate, methylene dianthranilate, and methylene dioleate) is described and the crystal structures discussed. The crystal packing of methylene dianthranilate is characterized by trimer formation due to hydrogen bonding via interactions between the hydrogen atom of the primary amine group and the oxygen of the carboxylic group.
Original languageAmerican English
Pages (from-to)744-750
Number of pages668
JournalCanadian Journal of Chemistry
DOIs
StatePublished - 1 Jan 2017

    Fingerprint

Cite this