4.3 Article

GREEN SYNTHESIS OF ALKANE BRIDGED BISIMIDAZOLIUM SALTS UNDER SOLVENT-FREE CONDITIONS

Journal

SYNTHETIC COMMUNICATIONS
Volume 42, Issue 3, Pages 380-387

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/00397911.2010.524960

Keywords

Bisimidazolium salts; N-arylimidazoles; N-heterocyclic carbenes; N-methylimidazoles; solvent-free

Funding

  1. SRF for ROCS, SEM, PAPD
  2. State Key Laboratory of Inorganic Synthesis and Preparative Chemistry at Jilin University [2009-06]
  3. Jiangsu Education Committee [08QLT001, 08QLD006]
  4. National Natural Science Foundation of China [21071121, 21172188, 21104064]

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A series of N-aryl or N-methyl substituted bisimidazolium dichloride or dibromide salts with different alkyl bridge lengths (n = 1-4) have been synthesized starting from N-arylimidazoles or N-methylimidazoles with dialkyl bromides or the less expensive but less reactive dialkyl chlorides under solvent-free conditions. This green protocol provided most bisimidazolium chloride and bromide salts in good yields, and the reaction time was shortened to a few hours. In two examples, we showed either bisimidazolium dichloride (1a) or dibromide salt (3c) can be easily converted to the corresponding dihexafluorophosphate salt (1a' or 3c') in near quantitative yield.

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