4.5 Article

The Ritter reaction under truly catalytic bronsted acid conditions

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2007, 期 28, 页码 4642-4645

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.200700562

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alcohols; amides; ritter reaction; homogeneous catalysis; bronsted acids

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Simple organic acids like 2,4-dinitrobenzenesulfonic acid (DNBSA) catalyze the Ritter reaction of secondary benzylic alcohols giving rise to the corresponding N-benzylacetamides in usually high yields. Reactions can be conducted without exclusion of oxygen and without the need of dry solvents. With tertiary alpha,alpha-dimethylbenzylic alcohols a different pathway involving a formal dimerization reaction takes place under the acid-catalytic conditions used. (C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)

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