Convenient preparation of 1,1-diacetates from aromatic aldehydes catalysed by zinc-montmorillonite

N. Nagy, Márta A. Jakab, József Kónya, S. Antus

Research output: Contribution to journalArticle

48 Citations (Scopus)

Abstract

1,1-Diacetates were produced from a variety of aromatic aldehydes using Zn-montmorillonite as a catalyst. The procedure generally resulted in good yields (98%) of aromatic aldehydes including those carrying electron donating- or withdrawing substituents. The great advantage of the application of Zn-montmorillonite catalyst is that the reaction takes place under mild conditions. In addition, the zinc cation exchanged form of montmorillonite has a minimal environmental impact.

Original languageEnglish
Pages (from-to)213-216
Number of pages4
JournalApplied Clay Science
Volume21
Issue number3-4
DOIs
Publication statusPublished - Jun 2002

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Bentonite
aldehyde
montmorillonite
Aldehydes
Zinc
zinc
catalyst
Catalysts
Environmental impact
Cations
environmental impact
cation
electron
Electrons

Keywords

  • 1,1-diacetates
  • Aromatic aldehydes
  • Catalysis
  • Zinc-montmorillonite

ASJC Scopus subject areas

  • Geochemistry and Petrology
  • Geology

Cite this

Convenient preparation of 1,1-diacetates from aromatic aldehydes catalysed by zinc-montmorillonite. / Nagy, N.; Jakab, Márta A.; Kónya, József; Antus, S.

In: Applied Clay Science, Vol. 21, No. 3-4, 06.2002, p. 213-216.

Research output: Contribution to journalArticle

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