Preparation method of indoxacarb intermediate

An intermediate, chlorindene technology, applied in the field of pesticide compound synthesis, can solve the problems of generating impurities, insufficient reaction, slow reaction speed, etc., and achieve the effect of speeding up the reaction speed and facilitating the reaction operation.

Active Publication Date: 2017-02-15
JINGBO AGROCHEM TECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] 7-chloroindeno[1,2-e][1,3,4]oxadiazine-2,4a(3H,5H)-dicarboxylic acid-4a-methyl-2-benzyl ester is mainly used in the synthesis of Insect agent indoxacarb, synthesized 7-chloroindeno[1,2-e][1,3,4]oxadiazine-2,4a(3H,5H)-dicarboxylic acid-4a-formazine in the prior art There are many process routes for ester-2-benzyl ester, and the reagents used are similar, but most of them vary with the design of the process route. In industrial production, other factors such as efficiency, yield or cost are quite different.
[0003] In the existing technology, the reaction solvent is generally ethylene dichloride, and the reaction of the intermediate 5-chloro-2-methoxycarbonyl-2-hydroxyl-1-indanone and benzyl carbazate generates water, in the presence of water In the cyclization reaction, the condensate will be decomposed into 5-chloro-2-methoxycarbonyl-2-hydroxy-1-indanone; and because the reaction solvent is dichloroethane, the reaction temperature is 83 ° C, and the by-product ethanol cannot Effective and timely separation, resulting in insufficient reaction and generation of impurities, resulting in the product 7-chloroin

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0020] (1) Add 20g (0.083mol) of 5-chloro-2-methoxycarbonyl-2-hydroxy-1-indanone to a 500ml clean anhydrous reaction bottle and dissolve it in xylene, then add 13.8g (0.083mol) of hydrazine Benzyl formate and 4.0 g (0.028 mol) of phosphorus pentoxide were controlled at a temperature of 50°C.

[0021] (2) Sampling and detection after 3 hours of reaction. When the raw material of the intermediate 5-chloro-2-methoxycarbonyl-2-hydroxy-1-indanone is normalized to ≤0.5%, add 41.6g (0.4mol) diethyl to the reaction solution Oxymethane.

[0022] (3) Put 100g of xylene on the tower for reflux. When the reaction temperature is 130°C, drop the reaction liquid from step (1) into the xylene, and control the reaction liquid to drop at a constant speed within 6-7 hours. When the temperature at the top of the tower is 78°C Start collecting by-product ethanol.

[0023] (4) After the collection of ethanol is completed, the reaction solution is subjected to negative pressure precipitation, the ...

Embodiment 2

[0025] 1) Add 20g (0.083mol) of 5-chloro-2-methoxycarbonyl-2-hydroxy-1-indanone to a 500ml clean and dry reaction bottle and dissolve it in xylene, then add 13.8g (0.083mol) of hydrazine Benzyl formate and 4.0g (0.028mol) phosphorus pentoxide, the temperature is controlled at 50°C.

[0026] (2) Sampling and detection after 3 hours of reaction. When the raw material of the intermediate 5-chloro-2-methoxycarbonyl-2-hydroxy-1-indanone is normalized to ≤0.5%, add 41.6g (0.4mol) diethyl to the reaction solution Oxymethane.

[0027] (3) Put 200g of xylene on the tower for reflux. When the reaction temperature is 140°C, drop the reaction liquid from step (1) into the xylene, and control the reaction liquid to drop at a constant speed within 6-7 hours. When the temperature at the top of the tower is 78°C Start collecting by-product ethanol.

[0028] (4) After the collection of ethanol is completed, the reaction solution is subjected to negative pressure precipitation, the reaction s...

Embodiment 3

[0030] (1) Dissolve 0.1 mol of the intermediate 5-chloro-2-methoxycarbonyl-2-hydroxy-1-indanone in xylene, then add 0.15 mol of benzyl carbazate and 0.05 mol of phosphorus pentoxide, 40 Reaction at ℃;

[0031] (2) Sampling and detection, when the intermediate 5-chloro-2-methoxycarbonyl-2-hydroxyl-1-indanone raw material is normalized to ≤0.5%, after separating the phosphoric acid in the lower layer, add diethyl to the reaction solution Oxymethane 0.6mol;

[0032] (3) The solvent xylene is refluxed in the rectification tower, and the reaction solution obtained in step (2) is dropped into the xylene in the rectification tower at a constant speed, and the xylene is controlled to be dripped at a constant speed of 6-7h, and the reaction temperature is at 140°C, when the top of the tower reaches the boiling point of ethanol at 78°C, start collecting ethanol at a speed of 1ml / s;

[0033] (4) When the boiling point of xylene is collected, the collection of ethanol is completed, and ...

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PUM

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Abstract

The invention relates to a preparation method of indoxacarb intermediate. The preparation method is characterized by comprising the following steps: dissolving intermediate 5-chloro-2-methoxycarbonyl-2-hydroxy-1-indanone into xylene, adding benzyl carbazate and phosphorus pentoxide, separating out phosphoric acid, adding diethoxymethane into reaction liquid, enabling the solvent xylene to flow back on a tower, dropping the obtained reaction liquid into xylene at a constant speed, gathering ethyl alcohol, performing negative pressure desolventizing on obtained reaction liquid, adding a crystallizing agent into the rest liquid, performing cooling crystallization, filtering, and drying, so as to obtain 7-chloroindeno [1,2-e][1,3,4] oxadiazine-2,4a (3H,5H)-dicarboxylicacid-4a-methyl-2-benzylester. The method is convenient to operate, increases the reaction temperature, accelerates the reaction speed, and obviously improves the content and the yield of the intermediate.

Description

technical field [0001] The invention relates to the technical field of pesticide compound synthesis, in particular to a preparation method of an indoxacarb intermediate. Background technique [0002] 7-chloroindeno[1,2-e][1,3,4]oxadiazine-2,4a(3H,5H)-dicarboxylic acid-4a-methyl-2-benzyl ester is mainly used in the synthesis of Insect agent indoxacarb, synthesized 7-chloroindeno[1,2-e][1,3,4]oxadiazine-2,4a(3H,5H)-dicarboxylic acid-4a-formazine in the prior art There are many ester-2-benzyl ester process routes, and the reagents used are similar, but most of them are different from the design of the process route. In industrial production, other factors such as efficiency or yield or cost are quite different. [0003] In the existing technology, the reaction solvent is generally ethylene dichloride, and the reaction of the intermediate 5-chloro-2-methoxycarbonyl-2-hydroxyl-1-indanone and benzyl carbazate generates water, in the presence of water In the cyclization reaction,...

Claims

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Application Information

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IPC IPC(8): C07D273/04
CPCC07D273/04
Inventor 李响韦能春戴荣华成道泉王建刚宋雪娇
Owner JINGBO AGROCHEM TECH CO LTD
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