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Reversible interconversion of N-nitroso (2-methylamino) acetonitrile and 3-methyl-5-amino-1, 2, 3-oxadiazolium chloride and related reactions

SK Vohra, GW Harrington, D Swern

文献索引:Vohra,S.K. et al. Journal of Organic Chemistry, 1978 , vol. 43, p. 1671 - 1673

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被引用次数: 5

摘要

Reaction of N-nitroso (2-methy1amino) acetonitrile (I) with gaseous hydrogen chloride in dry methanol, ethanol. or ether is a fast reaction that yields 3-methyl-5-amino-1, 2, 3- oxadiazolium chloride (VI) virtually quantitatively. A pathway for the conversion of I to VI involving anchimeric assistance by the nitroso group is suggested. With aqueous base at pH 8-11, VI is reversibly converted to I, but at pH 11.5-14 VI is converted to N-nitrososarcosine ...