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Updated: May 24, 2026

Facile Preparation of (2Z,4E)-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate
Published on: June 21, 2017
Acetaldehyde solid state reactivity at low temperature: formation of the acetaldehyde ammonia trimer
V Vinogradoff1, F Duvernay, M Farabet
1Laboratoire de Physique des Interactions Ioniques et Moléculaires, Centre St-Jérôme, Marseille, France. vassilissa.vinogradoff@etu.univ-provence.fr
Abstract:
We focus on low temperature reactivity from 25 to 300 K, in ice containing acetaldehyde, ammonia, and formic acid. We show that the warming of this ice mixture forms the acetaldehyde ammonia trimer (2,4,6-trimethyl-1,3,5-hexahydrotriazine, C(6)H(15)N(3)) after five steps. The reaction is monitored by FTIR spectroscopy and mass spectrometry. We propose a mechanism for its formation that differs from the one proposed in the liquid phase. The reaction intermediates, α-aminoethanol (from 80 K) and ethanimine (formed at 180 K), have been identified by a mechanistic approach: each step of the reaction has been treated separately. The chemical implications and the astrophysical relevance of the study are also discussed.
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