阅读说明：本技术 一种环磺酮产品的纯化方法 (Purification method of tembotrione product ) 是由 李林虎 许辉 石卫 李新生 孙敬权 许宜伟 孙丽梅 白光 钱敏 于 2020-04-09 设计创作，主要内容包括：一种环磺酮产品的纯化方法,方法包括以下步骤：1)将环磺酮产品溶解在含水溶液中,升温；2)加入吸附剂,进行保温、热过滤；3)控温调节含水溶液pH至3以下,降温、从溶液中结晶出纯化的环磺酮。本发明的磺酮产品的纯化方法,可大大降低磺酮产品中氰化物杂质的含量,提高了产品的纯度,通过将纯化前的环磺酮产品与纯化后的产品进行Ames检测,原本氰化物杂质含量由1327ppm降至100ppm以下。(A method of purifying a tembotrione product, the method comprising the steps of: 1) dissolving the tembotrione product in an aqueous solution, and heating; 2) adding adsorbent, and performing heat preservation and hot filtration; 3) regulating the pH value of the aqueous solution to be below 3 by controlling the temperature, reducing the temperature, and crystallizing the purified tembotrione from the solution. The method for purifying the sulfoketone product can greatly reduce the content of cyanide impurities in the sulfoketone product and improve the purity of the product, and the content of the cyanide impurities is reduced from 1327ppm to less than 100ppm originally by Ames detection of the cyclic sulfoketone product before purification and the purified product.)

1. A method of purifying a tembotrione product, the method comprising the steps of:

1) dissolving the tembotrione product in an aqueous solution, and heating;

2) adding adsorbent, and performing heat preservation and hot filtration;

3) regulating the pH value of the aqueous solution to be below 3 by controlling the temperature, reducing the temperature, and crystallizing the purified tembotrione from the solution.

2. The method for purifying the tembotrione product as claimed in claim 1, wherein said aqueous solution of step 1) is a mixture of acetonitrile, methanol, ethanol, dimethylformamide and water.

3. The method for purifying tembotrione product as claimed in claim 1 wherein said aqueous solution of step 1) contains from about 20% to about 40% water.

4. The method for purifying the tembotrione product as claimed in claim 1, wherein said step 1) of raising the temperature is carried out by raising the temperature to 30-60 ℃.

5. The method for purifying the tembotrione product as claimed in claim 1, wherein the time for said incubation in step 2) is between 0.2h and 1 h.

6. The method for purifying the tembotrione product of claim 1, further comprising, after step 2): and (3) carrying out extractive distillation on the organic solvent into an aqueous solution.

7. The process of claim 1, wherein the adsorbent is activated carbon or diatomaceous earth.

8. The process for purifying the tembotrione product of claim 1 wherein step 3) of temperature-controlled adjustment of the aqueous solution to a pH of less than 3 comprises adding hydrochloric acid to the aqueous solution to adjust the pH to less than 3.

9. The process of claim 8, further comprising adjusting the pH of the aqueous solution to less than 3 by adding hydrochloric acid.

10. The process for purifying the tembotrione product of claim 1 wherein in step 3) the agitation rate is from 150 to 200 revolutions.

Technical Field

The invention relates to the field of pesticide synthesis, in particular to a method for reducing the impurity level in a tembotrione product.

Background

The tembotrione is a triketone p-hydroxyphenylpyruvate dioxygenase (HPPD) inhibiting herbicide, and the HPPD inhibiting herbicide has the characteristics of high activity, low residue, safety to mammals, environmental friendliness and the like, so that the tembotrione becomes a good product in the corn herbicide market. The tembotrione has wide weeding spectrum and long weeding proper period, and the main targets are as follows: various broad-leaved weeds and grassy weeds in the middle and later-stage postemergence of the corn field have excellent control effects on thistle, field bindweed, speedwell, pepperweed, weasel, cleavers and the like, have no phytotoxicity on afterculture crops, and are one of the most important herbicides in the American corn field.

CAS number: 335104-84-2

The molecular formula is as follows: c₁₇H₁₆ClF₃O₆S

Molecular weight: 440.88

The chemical properties are as follows: white or off-white amorphous powders, which are hardly soluble in ethanol, very soluble in dichloromethane and slightly soluble in toluene.

Melting point: 123 (. degree. C.) has a structural formula of (formula 1):

the preparation of the tembotrione is that 2-chloro-3- (2,2, 2-trifluoroethoxy) methyl-4-methylsulfonylbenzoic acid reacts with thionyl chloride to generate 2-chloro-3- (2,2, 2-trifluoroethoxy) methyl-4-methylsulfonylbenzoyl chloride, then reacts with cyclohexanedione to generate enol ester, and finally generates tembotrione through acetone cyanohydrin rearrangement reaction. The reaction formula is as follows (formula 2):

the above-mentioned cyclosultone-forming product produced by rearrangement process usually produces acetone cyanohydrin as catalyst and contamination of reaction cyanide impurity, and positive Ames test experiment result can be obtained by contaminant mutagenicity detection (Ames), but this is not its inherent property, but is the result produced by residual cyanide impurity.

Disclosure of Invention

In order to solve the defects in the prior art, the invention aims to provide a method for purifying a tembotrione product, which solves the problem of an Ames test experiment of the tembotrione product and purifies the tembotrione product.

In order to achieve the above purpose, the purification method of the tembotrione product provided by the invention comprises the following steps:

1) dissolving the tembotrione product in an aqueous solution, and heating;

2) adding adsorbent, and performing heat preservation and hot filtration;

3) regulating the pH value of the aqueous solution to be below 3 by controlling the temperature, reducing the temperature, and crystallizing the purified tembotrione from the solution.

Further, the aqueous solution in step 1) is a solution obtained by mixing acetonitrile, methanol, ethanol, dimethylformamide and water.

Further, the water content in the aqueous solution in the step 1) is 20-40%.

Further, the temperature rise in the step 1) is to raise the temperature to 30-60 ℃.

Further, the heat preservation time in the step 2) is 0.2-1 h.

Further, after the step 2), the method further comprises the following steps: and (3) carrying out extractive distillation on the organic solvent into an aqueous solution.

Further, the adsorbent is activated carbon or diatomite.

Further, the step of adjusting the pH of the aqueous solution to be below 3 by controlling the temperature in the step 3) comprises adding hydrochloric acid into the aqueous solution to adjust the pH to be below 3.

Further, hydrochloric acid is added into the aqueous solution to adjust the pH value to be below 3.

Further, in the step 3), the stirring speed is 150 to 200 revolutions.

The method for purifying the sulfoketone product can greatly reduce the content of cyanide impurities in the sulfoketone product and improve the purity of the product, and the content of the cyanide impurities is reduced from 1327ppm to less than 100ppm originally by Ames detection of the cyclic sulfoketone product before purification and the purified product.

Detailed Description

The present invention will be described in further detail with reference to specific examples. It is to be understood that these examples are for the purpose of illustrating the general principles, essential features and advantages of the present invention, and that the present invention is not limited by the following examples, and that the conditions employed in the examples may be further modified according to specific requirements, and that the conditions not specified are generally conditions in routine experimentation.

The synthetic scheme includes the following:

2-chloro-3- (2,2, 2-trifluoroethoxy) methyl-4-methylsulfonylbenzoyl chloride and 1, 2-dichloroethane were added to a three-necked flask, and stirred while maintaining the temperature at 15 ℃. Thionyl chloride was added slowly. Reacting for 0.5h at normal temperature, heating to 75 ℃, and preserving heat for 3 h. The content of the raw materials is less than or equal to 0.2 percent through the central control detection, the solvent is evaporated to 85 ℃ under the reduced pressure of-0.098 mP, and the solvent and the excessive thionyl chloride are removed. Adding new 1, 2-dichloroethane and triethylamine again, adding 1,3 cyclohexanedione and acetone cyanohydrin, and keeping the temperature at 40 ℃ for 6 h. The detection reaction was complete. And filtering triethylamine salt, and concentrating under reduced pressure to obtain a reddish brown solid.

The synthetic reaction formula is shown as follows:

before the 2-chloro-3- (2,2, 2-trifluoroethoxy) methyl-4-methylsulfonylbenzoyl chloride reacts with cyclohexanedione, a proper amount of alkali such as triethylamine and the like can be added to form enol ester solution, and after the rearrangement reaction is finished, the cyclanone product is obtained through further distillation.