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This procedure has since been modified to give pure compound 7 in 39% overall yield (Holden, T. M.; Isovitsch, R. A.; Maverick, A. W. Unpublished work, 1995): the mixture of 7 and 1-bromo-8-chloroanthraquinone produced in the first KBr treatment was crystallized from hot nitrobenzene before the second treatment with KBr.
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9 was obtained as a ca. 10:1 mixture of 1,8-dibromo- and 1-bromo-8-chloroanthracenes, by starting from the corresponding 10:1 anthraquinone mixture and following the procedure reported by: Haenel, M. W.; Jakubik, D.; Kruger, C.; Betz, P. Chem. Ber. 1991, 124, 333.
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