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The Ritter Reaction under Truly Catalytic Brønsted Acid Conditions
85
Citations
33
References
2007
Year
Chemical EngineeringDerivativesRitter ReactionEngineeringIndustrial CatalysisFormal Dimerization ReactionNatural SciencesDiversity-oriented SynthesisCatalytic SynthesisSecondary Benzylic AlcoholsOrganic ChemistryCatalysisHomogeneous CatalysisChemistryMolecular CatalysisChemical KineticsSynthetic ChemistryBiomolecular Engineering
Abstract 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 α,α‐dimethylbenzylic alcohols a different pathway involving a formal dimerization reaction takes place under the acid‐catalytic conditions used. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)
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