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Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by Nitrates

In this paper, ferric nitrate was used to oxidize benzyl alcohol in a mild condition and demonstrated its better performance compared to HNO(3). In the reaction, the conversion rate and product selectivity could be both as high as 95% in N(2) atmosphere, while the benzaldehyde yield also reached 85%...

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Autores principales: Xu, Shurui, Wu, Jie, Huang, Peng, Lao, Chunwen, Lai, Hanchao, Wang, Yuxiong, Wang, Zhenyu, Zhong, Guoyu, Fu, Xiaobo, Peng, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7099050/
https://www.ncbi.nlm.nih.gov/pubmed/32266207
http://dx.doi.org/10.3389/fchem.2020.00151
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author Xu, Shurui
Wu, Jie
Huang, Peng
Lao, Chunwen
Lai, Hanchao
Wang, Yuxiong
Wang, Zhenyu
Zhong, Guoyu
Fu, Xiaobo
Peng, Feng
author_facet Xu, Shurui
Wu, Jie
Huang, Peng
Lao, Chunwen
Lai, Hanchao
Wang, Yuxiong
Wang, Zhenyu
Zhong, Guoyu
Fu, Xiaobo
Peng, Feng
author_sort Xu, Shurui
collection PubMed
description In this paper, ferric nitrate was used to oxidize benzyl alcohol in a mild condition and demonstrated its better performance compared to HNO(3). In the reaction, the conversion rate and product selectivity could be both as high as 95% in N(2) atmosphere, while the benzaldehyde yield also reached 85% in air. Similar to Fe(NO(3))(3)·9H(2)O, the other metallic nitrates such as Al(NO(3))(3)·9H(2)O and Cu(NO(3))(2)·3H(2)O could also oxidize the benzyl alcohol with high activity. The applicability of Fe(NO(3))(3)·9H(2)O for other benzylic alcohol was also investigated, and the reaction condition was optimized at the same time. The results showed the Fe(NO(3))(3)·9H(2)O would be more conducive in oxidizing benzyl alcohol under the anaerobic condition. The experiments in N(2) or O(2) atmospheres were conducted separately to study the catalytic mechanism of Fe(NO(3))(3). The results showed the co-existence of Fe(3+) and [Formula: see text] will generate high activity, while either was with negligible oxidation property. The cyclic transformation of Fe(3+) and Fe(2+) provided the catalytic action to the benzyl alcohol oxidation. The role of [Formula: see text] was also an oxidant, by providing HNO(2) in anaerobic condition, while [Formula: see text] would be regenerated from NO in aerobic condition. O(2) did not oxidize the benzyl alcohol conversion directly, while it could still be beneficial to the procedure by eliminating the unwelcome NO and simultaneously reinforcing the circulation of Fe(2+) and Fe(3+), which therefore forms a green cyclic oxidation. Hence, the benzyl alcohol oxidation was suggested in an air atmosphere for efficiency and the need of green synthesis.
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spelling pubmed-70990502020-04-07 Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by Nitrates Xu, Shurui Wu, Jie Huang, Peng Lao, Chunwen Lai, Hanchao Wang, Yuxiong Wang, Zhenyu Zhong, Guoyu Fu, Xiaobo Peng, Feng Front Chem Chemistry In this paper, ferric nitrate was used to oxidize benzyl alcohol in a mild condition and demonstrated its better performance compared to HNO(3). In the reaction, the conversion rate and product selectivity could be both as high as 95% in N(2) atmosphere, while the benzaldehyde yield also reached 85% in air. Similar to Fe(NO(3))(3)·9H(2)O, the other metallic nitrates such as Al(NO(3))(3)·9H(2)O and Cu(NO(3))(2)·3H(2)O could also oxidize the benzyl alcohol with high activity. The applicability of Fe(NO(3))(3)·9H(2)O for other benzylic alcohol was also investigated, and the reaction condition was optimized at the same time. The results showed the Fe(NO(3))(3)·9H(2)O would be more conducive in oxidizing benzyl alcohol under the anaerobic condition. The experiments in N(2) or O(2) atmospheres were conducted separately to study the catalytic mechanism of Fe(NO(3))(3). The results showed the co-existence of Fe(3+) and [Formula: see text] will generate high activity, while either was with negligible oxidation property. The cyclic transformation of Fe(3+) and Fe(2+) provided the catalytic action to the benzyl alcohol oxidation. The role of [Formula: see text] was also an oxidant, by providing HNO(2) in anaerobic condition, while [Formula: see text] would be regenerated from NO in aerobic condition. O(2) did not oxidize the benzyl alcohol conversion directly, while it could still be beneficial to the procedure by eliminating the unwelcome NO and simultaneously reinforcing the circulation of Fe(2+) and Fe(3+), which therefore forms a green cyclic oxidation. Hence, the benzyl alcohol oxidation was suggested in an air atmosphere for efficiency and the need of green synthesis. Frontiers Media S.A. 2020-03-20 /pmc/articles/PMC7099050/ /pubmed/32266207 http://dx.doi.org/10.3389/fchem.2020.00151 Text en Copyright © 2020 Xu, Wu, Huang, Lao, Lai, Wang, Wang, Zhong, Fu and Peng. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Xu, Shurui
Wu, Jie
Huang, Peng
Lao, Chunwen
Lai, Hanchao
Wang, Yuxiong
Wang, Zhenyu
Zhong, Guoyu
Fu, Xiaobo
Peng, Feng
Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by Nitrates
title Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by Nitrates
title_full Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by Nitrates
title_fullStr Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by Nitrates
title_full_unstemmed Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by Nitrates
title_short Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by Nitrates
title_sort selective catalytic oxidation of benzyl alcohol to benzaldehyde by nitrates
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7099050/
https://www.ncbi.nlm.nih.gov/pubmed/32266207
http://dx.doi.org/10.3389/fchem.2020.00151
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