Issue 13, 1984

N,N-bis(trimethylsilyl)methoxymethylamine as a convenient synthetic equivalent for +CH2NH2: primary aminomethylation of esters

Abstract

The introduction of a primary aminomethyl unit at the α-position of esters can be achieved in high yield by the silyl trifluoromethanesulphonate-catalysed reaction of ketene silyl acetals (2) with N,N-bis(trimethylsilyl)methoxymethylamine (1).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 883-884

N,N-bis(trimethylsilyl)methoxymethylamine as a convenient synthetic equivalent for +CH2NH2: primary aminomethylation of esters

K. Okano, T. Morimoto and M. Sekiya, J. Chem. Soc., Chem. Commun., 1984, 883 DOI: 10.1039/C39840000883

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