A copper-mediated reverse aromatic Finkelstein reaction in ionic liquid.

J Adv Res

Department of Chemical Engineering, Ho Chi Minh University of Technology, VNU-HCM, 268 Ly Thuong Kiet, District 10, Ho Chi Minh City, Viet Nam.

Published: March 2018

We have developed a general method for reverse aromatic Finkelstein reactions. Good reaction yields were obtained when aryl iodides or aryl bromides were treated with copper halide salts as promoters in a 1-butyl-3-methylimidazolium bromide ([BMIM]Br) ionic liquid (IL) solvent at 140 °C for 8 h. Preliminary investigation supported that the copper salts were also the halide sources in halogen exchange reactions. The optimized conditions are applicable to a variety of substrates and have excellent functional group tolerance. Additionally, the [BMIM]Br solvent showed good stability for at least 10 consecutive runs. Results indicated that the [BMIM]Br solvent was recyclable for reverse aromatic Finkelstein reactions.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057234PMC
http://dx.doi.org/10.1016/j.jare.2017.12.006DOI Listing

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