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Effect of Supercritical CO(2) as Reaction Medium for Selective Hydrogenation of Acetophenone to 1-Phenylethanol

[Image: see text] 1-Phenylethanol (PhE) is widely employed in the pharmaceutical industry as an anti-inflammatory and analgesic drug, as well as in chewing gums and yogurts as a food additive. In this work, we have investigated the selective synthesis of 1-phenylethanol (PhE) by hydrogenation of ace...

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Autores principales: More, Santosh R., Yadav, Ganapati D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644883/
https://www.ncbi.nlm.nih.gov/pubmed/31458874
http://dx.doi.org/10.1021/acsomega.8b00001
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author More, Santosh R.
Yadav, Ganapati D.
author_facet More, Santosh R.
Yadav, Ganapati D.
author_sort More, Santosh R.
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description [Image: see text] 1-Phenylethanol (PhE) is widely employed in the pharmaceutical industry as an anti-inflammatory and analgesic drug, as well as in chewing gums and yogurts as a food additive. In this work, we have investigated the selective synthesis of 1-phenylethanol (PhE) by hydrogenation of acetophenone using supercritical CO(2) as a solvent. Supercritical carbon dioxide (scCO(2)) replaces organic solvent because it is inexpensive, nontoxic, nonflammable, inert, and environmentally benign. Polyurea-based encapsulated mono- and bimetallic catalysts were synthesized and characterized using different characterization techniques. The effects of various reaction parameters, such as co-solvent, catalyst loading, hydrogen pressure, total scCO(2) pressure, and temperature, were studied to determine the reaction kinetics.
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spelling pubmed-66448832019-08-27 Effect of Supercritical CO(2) as Reaction Medium for Selective Hydrogenation of Acetophenone to 1-Phenylethanol More, Santosh R. Yadav, Ganapati D. ACS Omega [Image: see text] 1-Phenylethanol (PhE) is widely employed in the pharmaceutical industry as an anti-inflammatory and analgesic drug, as well as in chewing gums and yogurts as a food additive. In this work, we have investigated the selective synthesis of 1-phenylethanol (PhE) by hydrogenation of acetophenone using supercritical CO(2) as a solvent. Supercritical carbon dioxide (scCO(2)) replaces organic solvent because it is inexpensive, nontoxic, nonflammable, inert, and environmentally benign. Polyurea-based encapsulated mono- and bimetallic catalysts were synthesized and characterized using different characterization techniques. The effects of various reaction parameters, such as co-solvent, catalyst loading, hydrogen pressure, total scCO(2) pressure, and temperature, were studied to determine the reaction kinetics. American Chemical Society 2018-06-29 /pmc/articles/PMC6644883/ /pubmed/31458874 http://dx.doi.org/10.1021/acsomega.8b00001 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle More, Santosh R.
Yadav, Ganapati D.
Effect of Supercritical CO(2) as Reaction Medium for Selective Hydrogenation of Acetophenone to 1-Phenylethanol
title Effect of Supercritical CO(2) as Reaction Medium for Selective Hydrogenation of Acetophenone to 1-Phenylethanol
title_full Effect of Supercritical CO(2) as Reaction Medium for Selective Hydrogenation of Acetophenone to 1-Phenylethanol
title_fullStr Effect of Supercritical CO(2) as Reaction Medium for Selective Hydrogenation of Acetophenone to 1-Phenylethanol
title_full_unstemmed Effect of Supercritical CO(2) as Reaction Medium for Selective Hydrogenation of Acetophenone to 1-Phenylethanol
title_short Effect of Supercritical CO(2) as Reaction Medium for Selective Hydrogenation of Acetophenone to 1-Phenylethanol
title_sort effect of supercritical co(2) as reaction medium for selective hydrogenation of acetophenone to 1-phenylethanol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644883/
https://www.ncbi.nlm.nih.gov/pubmed/31458874
http://dx.doi.org/10.1021/acsomega.8b00001
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