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Published in 2017 at "Journal of Chemical Research"
DOI: 10.3184/174751917x14894997017379
Abstract: An economic four-step synthesis of 2,6-dimethoxy-1,4-benzoquinone was achieved in 68% overall yield starting from aniline. The reaction sequence involved conversion to 1,3,5-tribromoaniline, deamination, methoxylation, and oxidation. The procedure is operationally simple and amenable to scale-up…
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Keywords:
alternative synthesis;
synthesis dimethoxyl;
benzoquinone;
synthesis ... See more keywords