Ozonolytic synthesis of 2-hydroxybenzyl alcohol for the production of gastrodin

A. Halstian, A. Hasanova, H. Tarasenko
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Abstract

2-Hydroxybenzyl alcohol is an important active pharmaceutical ingredient for the production of many drugs, in particular gastrodin, which has a wide range of beneficial effects on epilepsy, Alzheimer’s disease, Parkinson’s disease, affective disorders, cerebral ischemia, cognitive disorders. It is known that 2- and 4-hydroxybenzyl alcohols and mixtures of both compounds are obtained by the interaction of phenol with formaldehyde in the presence of basic catalysts. Due to its high reactivity with formaldehyde, the isolation of pure compounds from the reaction mixtures obtained during the interaction of phenol with formaldehyde is a big problem. Isolation of 2-hydroxybenzyl alcohol in pure form from reaction mixtures is possible only using processes that cannot be carried out on an industrial scale and is accompanied by low yields of the target product. It is possible to get rid of these problems by means of the process of direct oxidation of the 2-hydroxytoluene with ozone in the liquid phase since methods of selective ozonation of methylbenzene to the oxygen derivatives are already known. Therefore, the development of a new low-temperature synthesis of 2-hydroxybenzyl alcohol using ozone is an urgent task. The aim of the work is to study the reaction of the oxidation of 2-hydroxytoluene by ozone in a solution of a stop reagent and catalytic impurities of compounds of transition metals and mineral acids for the development of a new method of synthesis of 2-hydroxybenzyl alcohol. Materials and methods. For the experiments, acetic anhydride of p. a. qualification was used; glacial acetic acid of puriss. qualification, which before use was purified by distillation under vacuum in the presence of potassium permanganate, 2-hydroxytoluene of puriss. Qualification, manganese (II) acetate of pur. Qualification, sulfuric and phosphoric acids of puriss. qualification. To determine the concentration of ozone in the gas phase, a spectrophotometric method was used, based on the measurement of the optical density of the gas flow in the UV region. For this purpose, a spectrophotometer SF-46 LOMO was used, in the measuring chamber of which a flow cuvette with quartz windows was installed. The material of the cuvette was Teflon. Continuous monitoring of the current concentration of ozone, with the recording of the analysis results in the form of a kinetic curve, was carried out when ozone-containing gas passed through the curette at a certain wavelength of a monochromatic light source. Results. The reaction of oxidation of 2-hydroxytoluene by ozone in a solution of the stop reagent – acetic anhydride was studied. It was shown that in the presence of sulfuric acid, it was possible to carry out direct ozonation of 2-hydroxytoluene to 2-hydroxybenzyl alcohol, which was formed in the kind of 2-acetoxybenzyl acetate with a yield of 13.0 %. The main products of the reaction under these conditions are aliphatic compounds, which are formed after the destruction of the aromatic ring. The selectivity of oxidation by alcohol was significantly increased when a catalyst – manganese (II) acetate – was added to the system. In its presence, a catalytic system As2O – H2SO4 – Mn(III) was created, which prevents ozonolysis and directed oxidation mainly to the methyl group of the substrate with the formation of 2-acetoxybenzyl acetate with a yield of 63.2 %. Conclusions. An environmentally friendly, low-temperature method for the synthesis of 2-hydroxybenzyl alcohol was developed by conducting the oxidation of 2-hydroxytoluene with ozone in a solution of the stop reagent – acetic anhydride in the presence of sulfuric acid and manganese (II) acetate.
臭氧分解法合成2-羟基苄基醇生产天麻素
2-羟基苄基醇是生产许多药物的重要活性药物成分,特别是天麻素,它对癫痫、阿尔茨海默病、帕金森病、情感性障碍、脑缺血、认知障碍具有广泛的有益作用。众所周知,2-和4-羟基苯基醇和这两种化合物的混合物是由苯酚与甲醛在碱性催化剂的存在下相互作用得到的。由于苯酚与甲醛的高反应活性,从苯酚与甲醛的反应混合物中分离出纯化合物是一个很大的问题。从反应混合物中分离出纯形式的2-羟基苄基醇,只能使用不能在工业规模上进行的工艺,并且伴随着目标产品的低收率。在液相中用臭氧直接氧化2-羟基甲苯的方法可以解决这些问题,因为已经有了选择性臭氧化甲苯生成氧衍生物的方法。因此,开发一种新的臭氧低温合成2-羟基苄基醇的方法是一项紧迫的任务。本工作的目的是研究臭氧在停止剂和过渡金属及无机酸化合物的催化杂质的溶液中氧化2-羟基甲苯的反应,以开发合成2-羟基苯甲醇的新方法。材料和方法。实验采用醋酸酐进行p.a.鉴定;纯冰醋酸。合格,使用前在高锰酸钾、纯化物2-羟基甲苯存在下真空蒸馏提纯。鉴定,pur (II)醋酸锰。纯化硫酸和磷酸的鉴定。资格。为了确定气相中臭氧的浓度,采用了分光光度法,基于测量气体流在紫外区的光密度。为此,使用了SF-46 LOMO分光光度计,在测量室中安装了石英窗的流动比色管。试管的材料是聚四氟乙烯。当含臭氧气体在单色光源的一定波长下通过管时,对臭氧的当前浓度进行连续监测,并以动力学曲线的形式记录分析结果。研究了臭氧在停止剂乙酸酐溶液中氧化2-羟基甲苯的反应。结果表明,在硫酸的存在下,2-羟基甲苯可以直接臭氧化生成2-羟基苄基醇,2-乙酰氧基苄基乙酸酯的收率为13.0%。在这些条件下反应的主要产物是脂肪族化合物,这些化合物是在芳环被破坏后形成的。在体系中加入醋酸锰,可显著提高醇氧化的选择性。在其存在下,建立了As2O - H2SO4 - Mn(III)催化体系,该体系防止臭氧分解,主要对底物的甲基进行定向氧化,生成2-乙酰氧基苄乙酸酯,产率为63.2%。在停止剂乙酸酐溶液中,在硫酸和醋酸锰的存在下,用臭氧氧化2-羟基甲苯,建立了一种环境友好的低温合成2-羟基苄基醇的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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