Abstract
Two methods for the synthesis of 2-tert.-butyl-8-hydroxyquinoline are described. One involves a direct reaction of the parent compound with tert.-butyl-lithium, and the other is based on a cyclization reaction of o-aminophenol with 3-chloro-4,4-dimethylpent-2-enal. Physical data confirming the structure of the compound are presented.
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