The first in situ synthesis of 1,3-dioxan-5-one derivatives and their direct use in Claisen-Schmidt reactions

Author:

Javad Poursharifi M.1,Mojtahedi Mohammad M.2,Saeed Abaee M.1,Hashemi Mohammad M.3

Affiliation:

1. Department of Chemistry, Science and Research Branch, Islamic Azad University, Tehran1477893855, Iran

2. Organic Chemistry Department, Chemistry and Chemical Engineering Research Center of Iran, P.O. Box 14335-186, Tehran, Iran

3. Department of Organic Chemistry, Faculty of Chemistry, Sharif University of Technology, Tehran113658639, Iran

Abstract

AbstractA method is developed for in situ generation of 1,3-dioxan-5-one derivatives 2. These compounds are simple precursors for accessing carbohydrate structures and previously had to be produced via stepwise procedures using excessive amounts of reagents. In the present work, three different derivatives of 2 were synthesized via the reaction of trialkoxyalkanes with dihydroxyacetone dimer 1 in the presence of acetic acid as the catalyst. In the same pot, derivatives of 2 were reacted with aromatic aldehydes and 30 mol% of pyrrolidine to obtain high yields of the respective bischalcones 3 within short time periods.

Publisher

Walter de Gruyter GmbH

Subject

Organic Chemistry

Reference68 articles.

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2. Direct organocatalytic de novo synthesis of carbohydrates;Angew. Chem. Int. Ed. Engl,2005

3. Infrared and raman studies of the dimeric structures of 1,3-dihydroxyacetone, d(+)- and dl-glyceraldehyde;J. Mol. Struct,1976

4. Cyclohexanones: evidence of chair inversion and estimate for barriers to planarity from the far-infrared spectra;Can. J. Chem,1983

5. Infrared and raman studies of the dimeric structures of 1,3-dihydroxyacetone, d(+)- and dl-glyceraldehyde;J. Mol. Struct,1976

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