The use of a modified Suzuki reaction for the synthesis of monoarylferrocenes

A modification of the Suzuki cross-coupling reaction proved to be a clean and useful method for the preparation of monosubstituted arylferrocenes. Iodoferrocene was reacted with a series of substituted arylboronic acids in the presence of sodium carbonate and palladium acetate in aqueous ethanol at...

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Vydáno v:Perkin transactions. 1 číslo 17; s. 2513 - 2523
Hlavní autoři: Imrie, C, Loubser, C, Engelbrecht, P, McCleland, CW
Médium: Journal Article
Jazyk:angličtina
Vydáno: CAMBRIDGE Royal Soc Chemistry 1999
Témata:
Chemistry
Chemistry, Organic
Physical Sciences
Science & Technology
HALOARENES
PALLADIUM
FERROCENE DERIVATIVES
CRYSTAL-STRUCTURE
BEHAVIOR
ARYLBORONIC ACIDS
ISSN:0300-922X
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Shrnutí:A modification of the Suzuki cross-coupling reaction proved to be a clean and useful method for the preparation of monosubstituted arylferrocenes. Iodoferrocene was reacted with a series of substituted arylboronic acids in the presence of sodium carbonate and palladium acetate in aqueous ethanol at room temperature to produce a range of substituted monoarylferrocenes. A systematic investigation undertaken to determine optimal reaction conditions indicated that scrupulous deoxygenation of the solvent is critical. The use of stronger bases such as barium hydroxide and potassium carbonate is favourable and gives rise to better yields of monoarylferrocenes. The reactions also proceed efficiently in aqueous DMF, broadening the scope of the reaction allowing efficient reactions with boronic acids that show low solubility in organic solvents.
ISSN:0300-922X
DOI:10.1039/a903058a