Novel preparation method of 2-thiopheneacetic acid

文档序号:1433975 发布日期:2020-03-20 浏览:54次 中文

阅读说明:本技术 一种新的2-噻吩乙酸的制备新方法 (Novel preparation method of 2-thiopheneacetic acid ) 是由 门希国 钱广 于 2019-12-09 设计创作,主要内容包括:本发明公开了一种新的2-噻吩乙酸的制备新方法,涉及医药中间体和精细化学品的合成技术领域,其制备原料包括噻吩和环氧乙烷,首先噻吩和环氧乙烷进行烷基化反应,烷基化反应中加入催化剂,生成2-噻吩乙醇后直接氧化制备2-噻吩乙酸,氧化过程中加入氧化剂,催化剂为无水氯化锌、无水氯化铝、三氟甲磺酸、浓硫酸的其中一种,其用量为原料摩尔数的0.1-0.3倍,优选催化剂为无水氯化锌,用量为原料的0.2倍摩尔数,所述氧化剂为高锰酸钾、过硫酸钾、臭氧的一种,优选为高锰酸钾。本发明通过噻吩和环氧乙烷进行烷基化反应,生成2-噻吩乙醇后直接氧化制备2-噻吩乙酸,具有原料成本低,反应路线短,生产工程三废排放量小等显著优势,适合进行大规模生产。(The invention discloses a novel preparation method of 2-thiopheneacetic acid, which relates to the technical field of synthesis of medical intermediates and fine chemicals, wherein the preparation raw materials comprise thiophene and ethylene oxide, firstly, the thiophene and the ethylene oxide are subjected to alkylation reaction, a catalyst is added in the alkylation reaction, 2-thiopheneethanol is generated and then is directly oxidized to prepare the 2-thiopheneacetic acid, an oxidant is added in the oxidation process, the catalyst is one of anhydrous zinc chloride, anhydrous aluminum chloride, trifluoromethanesulfonic acid and concentrated sulfuric acid, the dosage of the catalyst is 0.1-0.3 times of the molar number of the raw materials, the preferred catalyst is the anhydrous zinc chloride, the dosage of the catalyst is 0.2 times of the molar number of the raw materials, the oxidant is one of potassium permanganate, potassium persulfate and ozone, and the preferred potassium permanganate is potassium permanganate. The method prepares the 2-thiopheneacetic acid by directly oxidizing the thiophene and the ethylene oxide to generate the 2-thiopheneethanol through alkylation reaction, has the remarkable advantages of low raw material cost, short reaction route, small discharge amount of three wastes in production engineering and the like, and is suitable for large-scale production.)

1. A new method for preparing 2-thiopheneacetic acid is characterized in that raw materials comprise thiophene and ethylene oxide, firstly, the thiophene and the ethylene oxide are subjected to alkylation reaction, a catalyst is added in the alkylation reaction, 2-thiopheneethanol is generated and then is directly oxidized to prepare the 2-thiopheneacetic acid, and an oxidant is added in the oxidation process, wherein the specific preparation line is as follows:

Figure RE-DEST_PATH_IMAGE002A

2. the novel method for preparing 2-thiopheneacetic acid according to claim 1, wherein said catalyst is one of anhydrous zinc chloride, anhydrous aluminum chloride, trifluoromethanesulfonic acid and concentrated sulfuric acid, and is used in an amount of 0.1-0.3 times mole of the raw material, and preferably said catalyst is anhydrous zinc chloride and is used in an amount of 0.2 times mole of the raw material.

3. The novel method for preparing 2-thiopheneacetic acid according to claim 1, wherein said oxidizing agent is one of potassium permanganate, potassium persulfate and ozone, preferably potassium permanganate.

Technical Field

The invention relates to the technical field of synthesis of medical intermediates and fine chemicals, in particular to a novel preparation method of 2-thiopheneacetic acid.

Background

2-thiopheneacetic acid is a very important fine chemical and has very wide application in the fields of medicine, pesticide and other industries.

In the aspect of medicine, 2-thiopheneacetic acid is an intermediate of various cephalosporin antibiotics, and can also be used for preparing medicaments such as cardiovascular medicaments, lipid lowering medicaments, platelet coagulation inhibitors and the like; in the aspect of pesticides, 2-thiopheneacetic acid can be used for preparing various insecticides and herbicides and can also be used as a dye intermediate; in addition, the downstream derivative of 2-thiopheneacetic acid has wide application in the aspects of plastic additives and the like.

Currently, there are three main routes for the preparation of 2-thiopheneacetic acid:

route 1:

Figure 192495DEST_PATH_IMAGE001

route 2:

Figure 118862DEST_PATH_IMAGE002

route 3:

Figure 933235DEST_PATH_IMAGE003

in the route 1, after acetylation, a rephotography reaction is required to be carried out with strong ammonia water under the participation of sulfur and under high pressure, which relates to a high-pressure and high-risk process, and in addition, a large amount of high-sulfur and high-ammonia nitrogen wastewater can be generated, thereby bringing great environmental protection hidden trouble to production;

the first step of the route 2 is a chloromethylation reaction, the process can generate a large amount of mixed acid wastewater, the treatment difficulty is high, and the second step of the reaction uses virulent sodium cyanide, so that the potential safety hazard is great;

the second step of the route 3 needs to be oxidized by high lead acetate in the presence of boron trifluoride, and is a highly toxic and dangerous process, and the post-treatment of the lead-containing wastewater and waste materials has high treatment difficulty and high approval difficulty.

The three routes are combined to see that the existing production process of 2-thiopheneacetic acid has difficulties in environmental protection or safety, and the difficulties are difficult to overcome on the basis of no change of the original process route. Obviously, 2-thiopheneacetic acid is an extremely important medicine, pesticide and fine chemical, and an efficient, green and safe production process is urgently needed to be developed.

An effective solution to the problems in the related art has not been proposed yet.

Disclosure of Invention

The present invention is directed to a novel method for producing 2-thiopheneacetic acid, which solves the problems set forth in the background art.

In order to achieve the purpose, the invention provides the following technical scheme: a new method for preparing 2-thiopheneacetic acid, raw materials include thiophene and ethylene oxide, thiophene and ethylene oxide carry on the alkylation reaction at first, add catalyst in the alkylation reaction, produce 2-thiopheneethanol and then oxidize and prepare 2-thiopheneacetic acid directly, add oxidizing agent in the oxidation process, its preparation line specifically is as follows:

Figure RE-DEST_PATH_IMAGE005A

further, the oxidizing agent is one of potassium permanganate, potassium persulfate and ozone, and potassium permanganate is preferred.

Compared with the prior art, the invention has the following beneficial effects:

(1) the method prepares the 2-thiopheneacetic acid by directly oxidizing the thiophene and the ethylene oxide to generate the 2-thiopheneethanol through alkylation reaction, has the remarkable advantages of low raw material cost, short reaction route, small discharge amount of three wastes in production engineering and the like, and is suitable for large-scale production.

Detailed Description

The invention will be further described with reference to specific embodiments:

the catalyst for the alkylation with ethylene oxide in the invention can be one of anhydrous zinc chloride, anhydrous aluminum chloride, trifluoromethanesulfonic acid, concentrated sulfuric acid and other Lewis acids, and the dosage of the Lewis acid is 0.1-0.3 times of the mole number of the raw material, and the preferred catalyst is anhydrous zinc chloride, and the dosage of the Lewis acid is 0.2 times of the mole number of the raw material. The application of other Lewis acid catalysts which can be popularized according to industry knowledge, such as boron trifluoride, other metal chlorides and the like, obviously belongs to the protection scope of the invention; the oxidizing agent used in the oxidation reaction is one of potassium permanganate, potassium persulfate, ozone and other oxidizing agents, preferably potassium permanganate, and can be applied to other oxidizing agents which are generally popularized according to the industry, such as sodium hypochlorite, persulfate, percarbonate and the like, and obviously, the invention also belongs to the protection range; the core content of the invention is not affected by the adjustment of the conventional parameters in the reaction, such as the change of temperature and auxiliary raw materials, the change of reaction time, the replacement of solvent, and the update of post-treatment reagent and mode, and the invention belongs to the protection content of the invention.

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