Abstract
Conditions have been found for the mercuration of alkyl- and aryl- thiazoles. Mercuration takes place in position 5 of the ring, if it is free, and does not depend on the nature of the substituent in position 2. The possibility of the mercuration of a trisubstituted thiazole has been shown for the first time. When a phenyl radical is present in position 2, the mercury ion enters the para position of the phenyl nucleus.
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