Publication | Open Access
Benzamidomethylation with (Benzamidomethyl)triethylammonium Chloride. 2. A Simple Method for Benzamidomethylation of Thiols, Amines and Carboxylic Acids
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Citations
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References
2000
Year
Derivative (Chemistry)Carboxylic AcidsEngineeringTriethylammonium ChlorideBiochemistrySimple MethodNatural SciencesBenzamidomethyl ThioethersOrganic ChemistryWater SolutionStereoselective SynthesisChemistryChemical DerivativeSynthetic ChemistryBenzamidomethyl Esters Rcooch2nhbzBiomolecular Engineering
Thiols and amines were benzamidomethylated in water solution at room temperature with (benzamidomethyl)triethylammonium chloride (1) in the presence of a small quantity of triethylamine (pH>9). Benzamidomethyl thioethers (3a-d) and (benzamidomethyl) amines or di(benzamidomethyl)amines (5) were obtained in high yields (>90%) as well as S(CH2NHBz)2 in a reaction of 1 with Na2S. Benzamidomethyl esters RCOOCH2NHBz were obtained (60-75%) in reactions of carboxylic acids with 1 in chloroform or dioxane.
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