Synthesis and characterization of two new molten acid salts: Safe and greener alternatives to sulfuric acid for the hydrolytic conversion of 1,1,1,3-tetrachloro-3-phenylpropane to cinnamic acid

Available online Two new acid salts were synthesized, and their chemical structures were characterized by various spectra data analyses. Although 1H NMR did not show acid proton of [HSO4]−, the FTIR spectra of molten acid salts act as key support to approve of their chemical structures. The structur...

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Main Authors: Zaharani, Lia, Gorjian, Hayedeh, Johan, Mohd Rafie, Khaligh, Nader Ghaffari
Format: Article
Published: Elsevier 2021
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Online Access:http://eprints.um.edu.my/26077/
https://doi.org/10.1016/j.molstruc.2021.130977
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spelling my.um.eprints.260772021-12-29T02:55:40Z http://eprints.um.edu.my/26077/ Synthesis and characterization of two new molten acid salts: Safe and greener alternatives to sulfuric acid for the hydrolytic conversion of 1,1,1,3-tetrachloro-3-phenylpropane to cinnamic acid Zaharani, Lia Gorjian, Hayedeh Johan, Mohd Rafie Khaligh, Nader Ghaffari Q Science (General) Available online Two new acid salts were synthesized, and their chemical structures were characterized by various spectra data analyses. Although 1H NMR did not show acid proton of [HSO4]−, the FTIR spectra of molten acid salts act as key support to approve of their chemical structures. The structure elucidation of the molten acid salts demonstrated the existence of 4,4ʹ-trimethylene-N,Nʹ-dipiperidinium dication with sulfate and hydrogen sulfate anion(s). Thus, sulfuric acid can act as a diprotic or monoprotic Brönsted acid when it is treated by a secondary amine regarding the initial mole ratio of sulfuric acid and amine. Also, the catalytic activity of these molten acid salts was investigated for the hydrolytic conversion of (1,3,3,3-tetrachloropropyl)benzene to cinnamic acid. The desired product was obtained in 88 ± 2.0% yield under optimal conditions. The molten acid salts were high recyclable and their chemical structure and catalytic efficiency showed no significant change even after the 5th run. Furthermore, TMDP-SA (1:1) showed a much weaker corrosive property compared with TMDP-SA (1:2) and SA (98%), and the surface of stainless steel was intact even after 24 h. This fact and the acidity of two molten acid salts also confirm the proposed chemical structures. © 2021 Elsevier B.V. Elsevier 2021 Article PeerReviewed Zaharani, Lia and Gorjian, Hayedeh and Johan, Mohd Rafie and Khaligh, Nader Ghaffari (2021) Synthesis and characterization of two new molten acid salts: Safe and greener alternatives to sulfuric acid for the hydrolytic conversion of 1,1,1,3-tetrachloro-3-phenylpropane to cinnamic acid. Journal of Molecular Structure, 1245. p. 130977. ISSN 0022-2860 https://doi.org/10.1016/j.molstruc.2021.130977 doi:10.1016/j.molstruc.2021.130977
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic Q Science (General)
spellingShingle Q Science (General)
Zaharani, Lia
Gorjian, Hayedeh
Johan, Mohd Rafie
Khaligh, Nader Ghaffari
Synthesis and characterization of two new molten acid salts: Safe and greener alternatives to sulfuric acid for the hydrolytic conversion of 1,1,1,3-tetrachloro-3-phenylpropane to cinnamic acid
description Available online Two new acid salts were synthesized, and their chemical structures were characterized by various spectra data analyses. Although 1H NMR did not show acid proton of [HSO4]−, the FTIR spectra of molten acid salts act as key support to approve of their chemical structures. The structure elucidation of the molten acid salts demonstrated the existence of 4,4ʹ-trimethylene-N,Nʹ-dipiperidinium dication with sulfate and hydrogen sulfate anion(s). Thus, sulfuric acid can act as a diprotic or monoprotic Brönsted acid when it is treated by a secondary amine regarding the initial mole ratio of sulfuric acid and amine. Also, the catalytic activity of these molten acid salts was investigated for the hydrolytic conversion of (1,3,3,3-tetrachloropropyl)benzene to cinnamic acid. The desired product was obtained in 88 ± 2.0% yield under optimal conditions. The molten acid salts were high recyclable and their chemical structure and catalytic efficiency showed no significant change even after the 5th run. Furthermore, TMDP-SA (1:1) showed a much weaker corrosive property compared with TMDP-SA (1:2) and SA (98%), and the surface of stainless steel was intact even after 24 h. This fact and the acidity of two molten acid salts also confirm the proposed chemical structures. © 2021 Elsevier B.V.
format Article
author Zaharani, Lia
Gorjian, Hayedeh
Johan, Mohd Rafie
Khaligh, Nader Ghaffari
author_facet Zaharani, Lia
Gorjian, Hayedeh
Johan, Mohd Rafie
Khaligh, Nader Ghaffari
author_sort Zaharani, Lia
title Synthesis and characterization of two new molten acid salts: Safe and greener alternatives to sulfuric acid for the hydrolytic conversion of 1,1,1,3-tetrachloro-3-phenylpropane to cinnamic acid
title_short Synthesis and characterization of two new molten acid salts: Safe and greener alternatives to sulfuric acid for the hydrolytic conversion of 1,1,1,3-tetrachloro-3-phenylpropane to cinnamic acid
title_full Synthesis and characterization of two new molten acid salts: Safe and greener alternatives to sulfuric acid for the hydrolytic conversion of 1,1,1,3-tetrachloro-3-phenylpropane to cinnamic acid
title_fullStr Synthesis and characterization of two new molten acid salts: Safe and greener alternatives to sulfuric acid for the hydrolytic conversion of 1,1,1,3-tetrachloro-3-phenylpropane to cinnamic acid
title_full_unstemmed Synthesis and characterization of two new molten acid salts: Safe and greener alternatives to sulfuric acid for the hydrolytic conversion of 1,1,1,3-tetrachloro-3-phenylpropane to cinnamic acid
title_sort synthesis and characterization of two new molten acid salts: safe and greener alternatives to sulfuric acid for the hydrolytic conversion of 1,1,1,3-tetrachloro-3-phenylpropane to cinnamic acid
publisher Elsevier
publishDate 2021
url http://eprints.um.edu.my/26077/
https://doi.org/10.1016/j.molstruc.2021.130977
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score 13.214268