Nucleophilic Aromatic Substitution Reactions in Water Enabled by Micellar Catalysis.

Org Lett

Department of Chemistry & Biochemistry, University of California, Santa Barbara, California 93106, United States.

Published: October 2015

Given the huge dependence on dipolar, aprotic solvents such as DMF, DMSO, DMAc, and NMP in nucleophilic aromatic substitution reactions (SNAr), a simple and environmentally friendly alternative is reported. Use of a "benign-by-design" nonionic surfactant, TPGS-750-M, in water enables nitrogen, oxygen, and sulfur nucleophiles to participate in SNAr reactions. Aromatic and heteroaromatic substrates readily participate in this micellar catalysis, which takes place at or near ambient temperatures.

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Source
http://dx.doi.org/10.1021/acs.orglett.5b02240DOI Listing

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