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An efficient method for the preparation of tertiary esters by palladium-catalyzed alkoxycarbonylation of aryl bromides.

Organic letters (2011-12-16)
Zhuo Xin, Thomas M Gøgsig, Anders T Lindhardt, Troels Skrydstrup
RESUMEN

The palladium-catalyzed alkoxycarbonylation of aryl bromides is described for the efficient preparation of tertiary esters. The protocol proved compatible with a wide variety of functionalized (hetero)aromatic bromides, as well as several different sterically hindered tertiary alcohols, affording the alkoxycarbonylated products in high yields. Finally, the formation of aromatic trityl esters is discussed.

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Sigma-Aldrich
9-Methyl-9H-fluorene-9-carbonyl chloride, ≥99.0% (GC)
Sigma-Aldrich
9-Methyl-9H-fluorene-9-carbonyl-13C chloride, ≥97.0% (GC)