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The chemistry of N-substituted benzotriazoles. Part 1.1-(Chloromethyl)benzotriazole
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1987
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Chemical EngineeringDerivativesEngineeringHeterocyclicNatural SciencesDiversity-oriented SynthesisNew Benzotriazolium SaltsOrganic ChemistryN-chloromethyl GroupHigh YieldChemistryHeterocycle ChemistryHalogenationDerivative (Chemistry)N-substituted Benzotriazoles
The N-chloromethyl group of 1-(chloromethyl)benzotriazole undergoes nucleophilic substitution by carbon, nitrogen, phosphorus, oxygen, and sulphur nucleophiles. α-Lithiation was achieved in high yield in 1-phenylthiomethyl-, 1-phenylsulphinylmethyl-, and 1-(phenylstilphonylmethyl)benzotriazoles and the lithio derivatives reacted with a variety of electrophiles. New benzotriazolium salts were prepared by quaternization of the N-3 nitrogen with methyl iodide.