СATALYTIC METHOD FOR THE SYNTHESIS OF 3-HYDROXY-2-NAPHTOIC ACID ANILIDE

Arylamides of 3-hydroxy-2-naphthoic acid are widely used in the production of organic azo pigments, as medicines and pesticides. Titanium tetrachloride, tetrabutoxytitanium and polybutoxytitanates, previously used for the synthesis of the most important of them., 3-hydroxy-2-naphthoic acid anilide b...

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Дата:2022
Автор: Shteinberg, Leon
Формат: Стаття
Мова:English
Опубліковано: V.I.Vernadsky Institute of General and Inorganic Chemistry 2022
Онлайн доступ:https://ucj.org.ua/index.php/journal/article/view/487
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Назва журналу:Ukrainian Chemistry Journal

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Ukrainian Chemistry Journal
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spelling oai:ojs2.1444248.nisspano.web.hosting-test.net:article-4872022-12-30T12:24:36Z СATALYTIC METHOD FOR THE SYNTHESIS OF 3-HYDROXY-2-NAPHTOIC ACID ANILIDE Shteinberg, Leon phosphorus trichloride, antimony trifluoride, 3-hydroxy-2-naphthoic acid, benzoic acid, 3-hydroxy-2-naphthoic acid anilide, catalysis Arylamides of 3-hydroxy-2-naphthoic acid are widely used in the production of organic azo pigments, as medicines and pesticides. Titanium tetrachloride, tetrabutoxytitanium and polybutoxytitanates, previously used for the synthesis of the most important of them., 3-hydroxy-2-naphthoic acid anilide by boiling of the latter in aniline (184 °C), proved to be ineffective as catalysts in carrying out this reaction in ortho-xylene. The study of the reasons for this inhibition of catalysis showed that it can be associated with the interaction of Ti(4+) with the hydroxy group of 3-hydroxy-2-naphthoic acid, its oxidation, accompanied by a decrease in the effective charge of titanium. Taking into account this inhibition, in the search for new catalysts for the synthesis of 3-hydroxy-2-naphthoic acid anilide, the known literature data on the oxidizing ability (according to the values of the reaction rate constant k) with respect to phenoxyl radicals of a number of Lewis acids, including titanium tetrachloride, were used: SbCl5>TiCl4 >SnCl4>PCl5>AlCl3 k, l·mol-1·sec-1   105     157      156       42      18. This made it possible to choose phosphorus trichloride as an effective catalyst. It is shown that this compound, in an amount of only 2% mole. from 3-hydroxy-2-naphthoic acid, allows in boiling ortho-xylene (145 °C), under relatively mild conditions, compared to boiling aniline (184 °С), to obtain anilide 3-hydroxy-2-naphthoic acid (by reaction of the latter with aniline) of good quality with a practically quantitative yield. Antimony trifluoride also has similar pro­perties as a catalyst, at the level of efficiency of phosphorus trichloride. The ability of catalysts to act as an oxidizing agent should, apparently, always be taken into account during the catalytic amidation of aromatic oxycarboxylic acids at elevated temperatures. V.I.Vernadsky Institute of General and Inorganic Chemistry 2022-11-25 Article Article Organic chemistry Органическая xимия Органічна xімія application/pdf https://ucj.org.ua/index.php/journal/article/view/487 10.33609/2708-129X.88.10.2022.91-103 Ukrainian Chemistry Journal; Vol. 88 No. 10 (2022): Ukrainian Chemistry Journal; 91-103 Украинский химический журнал; Том 88 № 10 (2022): Ukrainian Chemistry Journal; 91-103 Український хімічний журнал; Том 88 № 10 (2022): Український хімічний журнал; 91-103 2708-129X 2708-1281 en https://ucj.org.ua/index.php/journal/article/view/487/251
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datestamp_date 2022-12-30T12:24:36Z
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language English
topic_facet phosphorus trichloride
antimony trifluoride
3-hydroxy-2-naphthoic acid
benzoic acid
3-hydroxy-2-naphthoic acid anilide
catalysis
format Article
author Shteinberg, Leon
spellingShingle Shteinberg, Leon
СATALYTIC METHOD FOR THE SYNTHESIS OF 3-HYDROXY-2-NAPHTOIC ACID ANILIDE
author_facet Shteinberg, Leon
author_sort Shteinberg, Leon
title СATALYTIC METHOD FOR THE SYNTHESIS OF 3-HYDROXY-2-NAPHTOIC ACID ANILIDE
title_short СATALYTIC METHOD FOR THE SYNTHESIS OF 3-HYDROXY-2-NAPHTOIC ACID ANILIDE
title_full СATALYTIC METHOD FOR THE SYNTHESIS OF 3-HYDROXY-2-NAPHTOIC ACID ANILIDE
title_fullStr СATALYTIC METHOD FOR THE SYNTHESIS OF 3-HYDROXY-2-NAPHTOIC ACID ANILIDE
title_full_unstemmed СATALYTIC METHOD FOR THE SYNTHESIS OF 3-HYDROXY-2-NAPHTOIC ACID ANILIDE
title_sort сatalytic method for the synthesis of 3-hydroxy-2-naphtoic acid anilide
description Arylamides of 3-hydroxy-2-naphthoic acid are widely used in the production of organic azo pigments, as medicines and pesticides. Titanium tetrachloride, tetrabutoxytitanium and polybutoxytitanates, previously used for the synthesis of the most important of them., 3-hydroxy-2-naphthoic acid anilide by boiling of the latter in aniline (184 °C), proved to be ineffective as catalysts in carrying out this reaction in ortho-xylene. The study of the reasons for this inhibition of catalysis showed that it can be associated with the interaction of Ti(4+) with the hydroxy group of 3-hydroxy-2-naphthoic acid, its oxidation, accompanied by a decrease in the effective charge of titanium. Taking into account this inhibition, in the search for new catalysts for the synthesis of 3-hydroxy-2-naphthoic acid anilide, the known literature data on the oxidizing ability (according to the values of the reaction rate constant k) with respect to phenoxyl radicals of a number of Lewis acids, including titanium tetrachloride, were used: SbCl5>TiCl4 >SnCl4>PCl5>AlCl3 k, l·mol-1·sec-1   105     157      156       42      18. This made it possible to choose phosphorus trichloride as an effective catalyst. It is shown that this compound, in an amount of only 2% mole. from 3-hydroxy-2-naphthoic acid, allows in boiling ortho-xylene (145 °C), under relatively mild conditions, compared to boiling aniline (184 °С), to obtain anilide 3-hydroxy-2-naphthoic acid (by reaction of the latter with aniline) of good quality with a practically quantitative yield. Antimony trifluoride also has similar pro­perties as a catalyst, at the level of efficiency of phosphorus trichloride. The ability of catalysts to act as an oxidizing agent should, apparently, always be taken into account during the catalytic amidation of aromatic oxycarboxylic acids at elevated temperatures.
publisher V.I.Vernadsky Institute of General and Inorganic Chemistry
publishDate 2022
url https://ucj.org.ua/index.php/journal/article/view/487
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