Thallium in organic synthesis. II. Acylation, aroylation, and tosylation of phenols and carboxylic acids
EC Taylor, GW McLay, A McKillop
Index: Taylor,E.C. et al. Journal of the American Chemical Society, 1968 , vol. 90, p. 2422 - 2423
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Citation Number: 47
Abstract
(0.11 mole) is stirred in 50 ml of petroleum ether and 0.10 mole of thallium (1) ethoxide added all at once. The mixture is stirred for 2-3 min, chilled, and filtered; the yield of acetylacetonatothallium (1) is quantitative; mp 160.5 o. 8-10 3-Methylpentane-2, 4-dione: A suspension of 0.10 mole of acetylacetonatothallium (1) in 85 ml of methyl iodide is heated under reflux with stirring for 4 hr, cooled, and filtered. The filtrate is passed through a short ...
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