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A Simple and Versatile Method for the Formation of Acetals/Ketals Using Trace Conventional Acids

[Image: see text] An important and surprising finding that the acetalization and ketalization of aldehydes and ketones with alcohols, respectively, proceed smoothly in the presence of 0.1 mol % acid, without removing water, has been presented. This process has many merits, such as commercial availab...

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Autores principales: Dong, Jian-Lian, Yu, Li-Si-Han, Xie, Jian-Wu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641695/
https://www.ncbi.nlm.nih.gov/pubmed/31458712
http://dx.doi.org/10.1021/acsomega.8b00159
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author Dong, Jian-Lian
Yu, Li-Si-Han
Xie, Jian-Wu
author_facet Dong, Jian-Lian
Yu, Li-Si-Han
Xie, Jian-Wu
author_sort Dong, Jian-Lian
collection PubMed
description [Image: see text] An important and surprising finding that the acetalization and ketalization of aldehydes and ketones with alcohols, respectively, proceed smoothly in the presence of 0.1 mol % acid, without removing water, has been presented. This process has many merits, such as commercial available catalysts with low cost and low loadings (as low as 0.03 mol %), quite a broad substrate scope (including various aldehydes, ketones, acid-sensitive substrates, and diols), a wide range of reaction temperature (−60 to 50 °C), high yields, large-scale preparation, environmental friendliness, and simple work-up procedure. This new protocol has also been successfully applied to protect the important organic compounds, such as 1,3-diols, 1,2-diols, acid-sensitive substrates, glucose, and 1,3-dicarbonyl compounds.
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spelling pubmed-66416952019-08-27 A Simple and Versatile Method for the Formation of Acetals/Ketals Using Trace Conventional Acids Dong, Jian-Lian Yu, Li-Si-Han Xie, Jian-Wu ACS Omega [Image: see text] An important and surprising finding that the acetalization and ketalization of aldehydes and ketones with alcohols, respectively, proceed smoothly in the presence of 0.1 mol % acid, without removing water, has been presented. This process has many merits, such as commercial available catalysts with low cost and low loadings (as low as 0.03 mol %), quite a broad substrate scope (including various aldehydes, ketones, acid-sensitive substrates, and diols), a wide range of reaction temperature (−60 to 50 °C), high yields, large-scale preparation, environmental friendliness, and simple work-up procedure. This new protocol has also been successfully applied to protect the important organic compounds, such as 1,3-diols, 1,2-diols, acid-sensitive substrates, glucose, and 1,3-dicarbonyl compounds. American Chemical Society 2018-05-07 /pmc/articles/PMC6641695/ /pubmed/31458712 http://dx.doi.org/10.1021/acsomega.8b00159 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 Dong, Jian-Lian
Yu, Li-Si-Han
Xie, Jian-Wu
A Simple and Versatile Method for the Formation of Acetals/Ketals Using Trace Conventional Acids
title A Simple and Versatile Method for the Formation of Acetals/Ketals Using Trace Conventional Acids
title_full A Simple and Versatile Method for the Formation of Acetals/Ketals Using Trace Conventional Acids
title_fullStr A Simple and Versatile Method for the Formation of Acetals/Ketals Using Trace Conventional Acids
title_full_unstemmed A Simple and Versatile Method for the Formation of Acetals/Ketals Using Trace Conventional Acids
title_short A Simple and Versatile Method for the Formation of Acetals/Ketals Using Trace Conventional Acids
title_sort simple and versatile method for the formation of acetals/ketals using trace conventional acids
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641695/
https://www.ncbi.nlm.nih.gov/pubmed/31458712
http://dx.doi.org/10.1021/acsomega.8b00159
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