Ab initio study of the base-promoted hydrolysis of N-methylformamide

Abstract

The intrinsic reaction coordinate (IRC) pathway for the base-promoted hydrolysis of N-methylformamide in the gas phase has been determined using ab initio molecular orbital calculations at the RHF/6-31+G(d) level of theory. Stationary points were reoptimized at the MP2 level. Along the IRC pathway, the initial process for the reaction is nucleophilic addition of the hydroxide to form a tetrahedral intermediate. The tetrahedral intermediate has to undergo conformational transitions before the reaction can proceed with the elimination step. Two channels for elimination were found; the preferred one leads to methylamide and formate anion, while the other leads to methylamide anion and formic acid. The reactants can also undergo spontaneous proton transfer to form N-methylformamidate anion and water. © 1995 American Chemical Society.

Department(s)

Chemistry and Biochemistry

Document Type

Article

DOI

https://doi.org/10.1021/j100034a012

Publication Date

1-1-1995

Journal Title

Journal of Physical Chemistry

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