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note
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When the temperature was raised up to 120°C, the major product was the dialkoxylation product, with a trace amount of the monoalkoxylation compound.
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note
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The submission of the purified symmetrical acetals (Figure 2) to conditions described for the formation of unsymmetrical acetals only results in a small amount of unsymmetrical acetals (for more details, please see SI). This observation supports our proposed mechanism that the reaction does favor a sequential double C-H alkoxylation procedure, but not another pathway such as potential acetal exchange.
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