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DePaul University

Investigation of montmorillonite clay-mediated reactions of aldehydes

Abstract

dc:description.abstract

Montmorillonite clays are employed as effective and environmentally benign heterogeneous catalysts for several reactions of aldehydes: (1) the hetero-Diels-Alder reaction of aromatic aldehydes with 2,3-dimethyl-1,3-butadiene to give dihydropyran products; (2) the cyclotrimerization of aliphatic aldehydes; (3) the oxidation of aliphatic aldehydes to the corresponding carboxylic acids; (4) the addition of allyltrimethylsilane to electron deficient benzaldehydes to give homoallylic silyl ethers. The hetero-Diels-Alder and allyl silation reactions are effected in the presence of heat- activated Montmorillonite K10 clay, at room temperature or below, in the presence of minimal solvent. A temperature dependent equilibrium is observed for the cyclotrimerization of aliphatic aldehydes in the presence of untreated Montmorillonite K10, while aerobic oxidation to the carboxylic acids is observed in the presence of Montmorillonite KSF.

Degree

thesis:*
Level thesis:degree_level
Thesis
Discipline thesis:degree_discipline
Chemistry
Year dc:date.available
2009

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Mondjinou, Yawo A.

Subjects

dc:subject × 5

Identifiers

dc:identifier.*
Repository record dc:identifier
https://via.library.depaul.edu/etd/6
OAI identifier oai:identifier
oai:via.library.depaul.edu:etd-1006

Chain of custody

source
Harvested from
DePaul University
Base URL
via.library.depaul.edu/do/oai/
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Mondjinou, Yawo A.. Investigation of montmorillonite clay-mediated reactions of aldehydes. Thesis thesis, 2009. https://via.library.depaul.edu/etd/6