KANNER, C. B.;PANDIT, U. K., TETRAHEDRON, 1982, 38, N 24, 3597-3604
作者:KANNER, C. B.、PANDIT, U. K.
DOI:——
日期:——
A Method for the Preparation of β-Amino-α,β-unsaturated Carbonyl Compounds: Study of Solvent Effect and Mechanism
作者:Reyno R. S.、Akash Sugunan、Ranganayakulu S.、Cherumuttathu H. Suresh、Goreti Rajendar
DOI:10.1021/acs.orglett.9b04531
日期:2020.2.7
An efficient method for the preparation of β-amino-α,β-unsaturated carbonylcompounds is demonstrated. Bench-stable sodium 3-oxo-enolates were prepared from carbonylcompounds, and reacted with amines in the presence of an acid and a desiccant. DFT studies revealed contrasting mechanisms toward the reactivity of aliphatic amines in protic solvents and aromatic amines in aprotic solvents. While the
benzyl bromide 2 and cinnamyl bromide 3 give products which are dependent both upon the nature of the amine component of the enamine and, in the case of the amides, upon the amine from which the amide is derived. The β-enamino esters react with benzyl bromide to yield predominantly dialkylated products in the case of the pyrrolidine ester 1a. Reactions of the same esters with cinnamyl bromide yield