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• W2040924163 abstract "N,N-Dialkyl aromatic amines with a variety of ring substituents are N-dealkylated and N-nitrosated efficiently by n-butyl nitrite/ammonium chloride/water at reflux temperature. Ring nitrosation was never observed, but minor amounts of m- and p-nitro amines and/or nitrosamines were formed in some cases. Ring nitration is rather a reaction of the initial substrate than a process occurring on formed nitrosamines. The leaving propensities of the initial N-substituents to yield nitrosamines were in the order benzyl methyl alkyl." @default.
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• W2040924163 date "1991-09-01" @default.
• W2040924163 modified "2023-10-12" @default.
• W2040924163 title "N-Dealkylation-N-nitrosation of tertiary aromatic amines by N-butyl nitrite" @default.
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• W2040924163 doi "https://doi.org/10.1016/s0040-4020(01)81940-2" @default.
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