Heterogeneous catalytic reduction of substituted 5-acyl-1,3-dioxanes

Objectives. To study the hydrogenation of substituted 5-acyl-1,3-dioxanes in the presence of metal-containing catalysts (Pt/Re, Pd/C, Ni/kieselguhr, and Ni/Mo).Methods. In order to determine the qualitative and quantitative composition of the reaction masses, the following analysis methods were used...

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Main Authors: A. I. Musin, Yu. G. Borisova, G. Z. Raskil’dina, R. R. Daminev, A. R. Davletshin, S. S. Zlotskii
Format: Article
Language:Russian
Published: MIREA - Russian Technological University 2022-07-01
Series:Тонкие химические технологии
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Online Access:https://www.finechem-mirea.ru/jour/article/view/1837
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author A. I. Musin
Yu. G. Borisova
G. Z. Raskil’dina
R. R. Daminev
A. R. Davletshin
S. S. Zlotskii
author_facet A. I. Musin
Yu. G. Borisova
G. Z. Raskil’dina
R. R. Daminev
A. R. Davletshin
S. S. Zlotskii
author_sort A. I. Musin
collection DOAJ
description Objectives. To study the hydrogenation of substituted 5-acyl-1,3-dioxanes in the presence of metal-containing catalysts (Pt/Re, Pd/C, Ni/kieselguhr, and Ni/Mo).Methods. In order to determine the qualitative and quantitative composition of the reaction masses, the following analysis methods were used: gas-liquid chromatography (using the Kristall 2000 hardware complex); mass-spectroscopy (using Chromatec-Kristall 5000M device with NIST 2012); nuclear magnetic resonance (NMR) spectrometry (using Bruker AM-500 device with operating frequencies of 500 and 125 MHz).Results. Hydrogenation of substituted 5-acyl-1,3-dioxanes obtained by condensation of carbonyl compounds with paraformaldehyde and sulfuric acid was used to synthesize heterocyclic alcohols in the presence of metal-containing catalysts with a conversion of the initial ketones of 60–90% and a formation selectivity of target products of 70–90%. Substances were analyzed and confirmed by gas-liquid chromatography, mass spectrometry and NMR spectroscopy.Conclusions. The best catalyst for the reduction of substituted 5-acyl-1,3-dioxanes is Pd/C. By using this catalyst, it is possible to achieve a high selectivity for the formation of the corresponding heterocyclic alcohols at a conversion rate of the initial ketones of 60–90%.
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institution Kabale University
issn 2410-6593
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publisher MIREA - Russian Technological University
record_format Article
series Тонкие химические технологии
spelling doaj-art-37e87ed355694bdc9caa90e70ea5826c2025-08-20T03:56:32ZrusMIREA - Russian Technological UniversityТонкие химические технологии2410-65932686-75752022-07-0117320120910.32362/2410-6593-2022-17-3-201-2091679Heterogeneous catalytic reduction of substituted 5-acyl-1,3-dioxanesA. I. Musin0Yu. G. Borisova1G. Z. Raskil’dina2R. R. Daminev3A. R. Davletshin4S. S. Zlotskii5Institute of Chemical Technology and Engineering, Ufa State Petroleum Technological University, SterlitamakUfa State Petroleum Technological UniversityUfa State Petroleum Technological UniversityUfa State Petroleum Technological UniversityUfa State Petroleum Technological UniversityUfa State Petroleum Technological UniversityObjectives. To study the hydrogenation of substituted 5-acyl-1,3-dioxanes in the presence of metal-containing catalysts (Pt/Re, Pd/C, Ni/kieselguhr, and Ni/Mo).Methods. In order to determine the qualitative and quantitative composition of the reaction masses, the following analysis methods were used: gas-liquid chromatography (using the Kristall 2000 hardware complex); mass-spectroscopy (using Chromatec-Kristall 5000M device with NIST 2012); nuclear magnetic resonance (NMR) spectrometry (using Bruker AM-500 device with operating frequencies of 500 and 125 MHz).Results. Hydrogenation of substituted 5-acyl-1,3-dioxanes obtained by condensation of carbonyl compounds with paraformaldehyde and sulfuric acid was used to synthesize heterocyclic alcohols in the presence of metal-containing catalysts with a conversion of the initial ketones of 60–90% and a formation selectivity of target products of 70–90%. Substances were analyzed and confirmed by gas-liquid chromatography, mass spectrometry and NMR spectroscopy.Conclusions. The best catalyst for the reduction of substituted 5-acyl-1,3-dioxanes is Pd/C. By using this catalyst, it is possible to achieve a high selectivity for the formation of the corresponding heterocyclic alcohols at a conversion rate of the initial ketones of 60–90%.https://www.finechem-mirea.ru/jour/article/view/1837hydrogenation5-acyl-1,3-dioxanesheterocyclic alcoholscatalysts pt/re, pd/c, ni/kieselguhr, ni/mo
spellingShingle A. I. Musin
Yu. G. Borisova
G. Z. Raskil’dina
R. R. Daminev
A. R. Davletshin
S. S. Zlotskii
Heterogeneous catalytic reduction of substituted 5-acyl-1,3-dioxanes
Тонкие химические технологии
hydrogenation
5-acyl-1,3-dioxanes
heterocyclic alcohols
catalysts pt/re, pd/c, ni/kieselguhr, ni/mo
title Heterogeneous catalytic reduction of substituted 5-acyl-1,3-dioxanes
title_full Heterogeneous catalytic reduction of substituted 5-acyl-1,3-dioxanes
title_fullStr Heterogeneous catalytic reduction of substituted 5-acyl-1,3-dioxanes
title_full_unstemmed Heterogeneous catalytic reduction of substituted 5-acyl-1,3-dioxanes
title_short Heterogeneous catalytic reduction of substituted 5-acyl-1,3-dioxanes
title_sort heterogeneous catalytic reduction of substituted 5 acyl 1 3 dioxanes
topic hydrogenation
5-acyl-1,3-dioxanes
heterocyclic alcohols
catalysts pt/re, pd/c, ni/kieselguhr, ni/mo
url https://www.finechem-mirea.ru/jour/article/view/1837
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AT gzraskildina heterogeneouscatalyticreductionofsubstituted5acyl13dioxanes
AT rrdaminev heterogeneouscatalyticreductionofsubstituted5acyl13dioxanes
AT ardavletshin heterogeneouscatalyticreductionofsubstituted5acyl13dioxanes
AT sszlotskii heterogeneouscatalyticreductionofsubstituted5acyl13dioxanes