Chemischer Informationsdienst
 1974
DOI: 10.1002/chin.197441177
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ChemInform Abstract: SYNTHESE UND REAKTIONEN VON AETHYLIDEN‐METHYLSUCCINIMID

Siegrid Schoch1,
Gerhard Klein2,
U. Linsenmeier3
et al.

Abstract: Brom‐propionsäureester (I) und Acetessigester (II) reagieren in Gegenwart von Alkali zunächst zu (III), das durch Behandlung mit Boranat und dann mit Ammoniak zu dem substituierten Imid (IVa) führt.Mit Thionylchlorid entsteht die Chlor:‐ verbindung (IVb), die mit Ammoniak (V) gibt.

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