Registration Number
0210U003246,
0107U001102
, R & D reports
Title
Elaboration theoretical and practical basis of a-alkylacrolein dimers derivatives synthesis
popup.stage_title
Head
Marshalok Galina,
Registration Date
27-01-2010
Organization
Lviv Polytechnic National University
popup.description2
The quantum-chemical ground of joint synthesis mechanism of sodium salts of 2,5-dimethyl- and 2,5-diethyl-3,4-dihydro-2Н-pyran-2-carboxylic acids and 2,5-dimethyl- and 2,5-diethyl-3,4-dihydro-2H-pyran-2-methanols is first conducted on the Cannizzaro reaction by the semiempiric program MOPAC2009 in different solvents. The methods of synthesis and analytical control are developed, influence of temperature on speed of reaction and output products is studied. The optimum terms of synthesis are set and the laboratory standards of 2,5-dimethyl- and 2,5-diethyl-3,4-dihydro-2Н-pyran-2-carboxylic acids and their sodium salts and 2,5-dimethyl- and 2,5-diethyl-3,4-dihydro-2H-pyran-2-methanols are got on the Cannizzaro reaction. The structures of the synthesized matters are confirm by the IR- and NMR-spectroscopies methods. It was set by the single-crystal X-ray method, that a molecule of 2,5-dimethyl-3,4-dihydro-2Н-pyran-2-carboxylic acid is as an armchair of endo-diasteromer. Character of placing of peaks on the diffractograms of X-ray analysis of sodium salts powders of 2,5-dimethyl- and 2,5-diethyl-3,4-dihydro-2Н-pyran-2-carboxylic acids and their intensity specifies that they are isostructuric and have a similar molecular structure. It is set that the a-alkylacrolein dimers and their alcoholic derivatives have high biological ability, which will allow to use them for obtaining new national veterinary drugs.
Product Description
popup.authors
Карп'як Наталія Миронівна
Ковальський Ярослав Петрович
Полюжин Ігор Петрович
Федевич Марія Дмитрівна
Ятчишин Йосип Йосипович
popup.nrat_date
2020-04-02