OBTAINING ALKENE DERIVATIVES OF CHITIN

This article presents the results of obtaining an alkene derivative of chitin from a chitin biopolymer.Chitin from a crab shell was used for the reaction in the work.The reaction was carried out in the presence of EDC, NHS, and DMAP.Acrylic acid was first used to introduce a double bond into the chitin molecule.It was found that at 20-40C the reaction does not occur, and at 50C the reaction follows the Michael reaction path.Then, using the same method, a reaction was carried out with but-3-enoic acid.Using a less electrophilic acid, the expected compound was obtainedThe article concludes that to obtain an alkene derivative of chitin, it is necessary to use a less electrophilically activated acid to ensure the reaction proceeds in the desired direction.The structure of the compound was identified using nuclear magnetic resonance.

Publication Details

Journal
BSU- Journal of Chemistry and Material Sciences
Published
2025-01-01
DOI
https://doi.org/10.30546/209501.201.2024.1.04.057
Primary Topic
Carbohydrate Chemistry and Synthesis
Type
article
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article

OBTAINING ALKENE DERIVATIVES OF CHITIN

BSU- Journal of Chemistry and Material Sciences
Carbohydrate Chemistry and Synthesis
article

OBTAINING ALKENE DERIVATIVES OF CHITIN

article en

Abstract

This article presents the results of obtaining an alkene derivative of chitin from a chitin biopolymer.Chitin from a crab shell was used for the reaction in the work.The reaction was carried out in the presence of EDC, NHS, and DMAP.Acrylic acid was first used to introduce a double bond into the chitin molecule.It was found that at 20-40C the reaction does not occur, and at 50C the reaction follows the Michael reaction path.Then, using the same method, a reaction was carried out with but-3-enoic acid.Using a less electrophilic acid, the expected compound was obtainedThe article concludes that to obtain an alkene derivative of chitin, it is necessary to use a less electrophilically activated acid to ensure the reaction proceeds in the desired direction.The structure of the compound was identified using nuclear magnetic resonance.

BSU- Journal of Chemistry and Material Sciences
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Carbohydrate Chemistry and Synthesis
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