Abstract
The mechanism of N-methylformamide metathesis with dimethyl carbonate, which leads to the formation of N,O-dimethyl carbamate, is studied using the quantum-chemical B3LYP/6-311++G(df,p) approach. The reaction consists of three stages: the conversion of formamide to iminol; the adding of dimethyl carbonate at the azomethine bond of iminol; and decomposition of the resulting product into carbamate and methyl formate. The second stage limits the rate of interaction. All stages proceed through concerted cyclic transition state, and all of them are catalyzed efficiently by a monomer and a dimer of methanol.
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