JOURNAL ARTICLE

Synthesis of Acrylamides\nvia the Doebner–Knoevenagel\nCondensation

Michael J. Zacuto (1734769)

Year: 2019 Journal:   OPAL (Open@LaTrobe) (La Trobe University)   Publisher: La Trobe University

Abstract

A selective\nsynthesis of acrylamides had been developed using the\nDoebner–Knoevenagel condensation. The reaction occurs under\nmild conditions at ambient temperatures, tolerates a wide array of\nfunctional groups, and affords the <i>E</i>-isomer with\nhigh selectivity. The reported method expands the scope of this classic\nreaction to a class of industrially important products and as well\nas to the use of aliphatic aldehydes. An organocatalytic mechanism\nhas been proposed, and the ability to scale the process has been demonstrated.

Keywords:
Scope (computer science) Process (computing) Scale (ratio) Class (philosophy) Process development Reaction conditions

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Topics

Organic and Inorganic Chemical Reactions
Physical Sciences →  Chemistry →  Spectroscopy
Synthesis of heterocyclic compounds
Physical Sciences →  Chemistry →  Organic Chemistry
Multicomponent Synthesis of Heterocycles
Physical Sciences →  Chemistry →  Organic Chemistry

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