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Using 4-bromo-2-tert-butylphenol or 2-tert-butylphenol as starting materials, this synthetic method of 2(3H)-benzofuranones could not proceed cleanly, and only trace amounts of benzofuranone derivatives (6% and 5% yield, respectively) were obtained. We thus decided that the benzaldehyde derivative 3b would be led by oxidation of a benzylic methyl group.
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