Reported herein is a safe and economical
synthesis of methyl 6-chloro-5-(trifluoromethyl)nicotinate,
an intermediate in the synthesis of novel anti-infective agents. The
key to this process is the trifluoromethylation of an aryl iodide
using an inexpensive methyl chlorodifluoroacetate (MCDFA)/KF/CuI system,
with an emphasis on the development work which led to this effective
process
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