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A kind of synthetic method of L-type glufosinate-ammonium ammonium salt

A synthetic method and technology of ammonium phosphonate, applied in the field of synthesis of L-type glufosinate-ammonium ammonium salt, can solve the problems of dimer formation, high price, low yield, etc., achieve simple process flow, improve weed control High efficacy and high yield

Active Publication Date: 2017-11-07
JIANGSU SEVENCONTINENT GREEN CHEM CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0010] The actual yields of the above 1, 2, and 4 methods are far below the reported yields, the waste of raw materials is large, the yield is low, and the pollution is serious, and the actual raw material cost is higher than the selling price of L-glufosinate-ammonium on the market. It's much higher, it doesn't make economic sense
[0011] Method 3 is a traditional classic method, and may have been industrialized in Meiji Fruit Industry Co., Ltd., but the total yield is only about 30%. The key is that the intermediate step α-butyronic acid is very easy to decarboxylate in the acid water hydrolysis process, and It is easy to form dimers, so the yield is also very low. Although the route is simple, it is not economical

Method used

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  • A kind of synthetic method of L-type glufosinate-ammonium ammonium salt
  • A kind of synthetic method of L-type glufosinate-ammonium ammonium salt
  • A kind of synthetic method of L-type glufosinate-ammonium ammonium salt

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Experimental program
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Effect test

Embodiment 1

[0039] Add 23.3 grams of 4-(ethoxy-(methyl)phosphinyl)-2-acetoxybutyrocyanide to 73 grams of 15% hydrochloric acid, heat and reflux at 80°C for 4 hours, and wait for the raw materials to react completely The acid water was distilled off under reduced pressure, then cooled to room temperature, methanol was added, stirred, and the ammonium chloride formed was filtered off, and the methanol filtrate was distilled off under negative pressure at 20°C. Add water and sodium hydroxide to the residue to neutralize to obtain disodium salt, then add 0.117 grams of catalyst ruthenium oxide, add dropwise 59.6 grams of 15% content of new sodium hypochlorite under stirring, control the temperature at about 30 ° C to complete the dropwise addition, and keep the temperature for 3 hours. After the oxidation reaction is basically completed, the catalyst is filtered out, most of the water is distilled off under negative pressure, then acetone is added, hydrogen chloride gas is introduced to neutra...

Embodiment 2

[0041]Add 23.3 grams of 4-(ethoxy-(methyl)phosphinyl)-2-acetoxybutyrocyanide to 73 grams of 15% hydrochloric acid, heat and reflux at 80°C for 6 hours, after the reaction of the raw materials is complete The acid water was distilled off under reduced pressure, then cooled to normal temperature, methanol was added, stirred, and the ammonium chloride formed was filtered off, and methanol was distilled off the methanol filtrate under negative pressure at 15°C. Add water and sodium hydroxide to the residue to neutralize to obtain disodium salt, then add 0.163 g of catalyst ruthenium oxide, add dropwise 74.5 g of 20% fresh sodium hypochlorite with stirring, control the temperature at about 40°C to complete the dropwise addition, and keep the temperature for 4 hours. After the oxidation reaction is basically completed, the catalyst is filtered out, most of the water is distilled off under negative pressure, then acetone is added, hydrogen chloride gas is introduced to neutralize the ...

Embodiment 3

[0043] Add 23.3 grams of 4-(ethoxy-(methyl)phosphinyl)-2-acetoxybutyrocyanide to 146 grams of 10% hydrochloric acid, heat and reflux at 100°C for 8 hours, and wait for the raw materials to react completely The acid water was distilled off under reduced pressure, then cooled to normal temperature and methanol was added, stirred, and the ammonium chloride formed was filtered off, and the methanol filtrate was distilled off methanol under negative pressure at 20°C. Add water and sodium hydroxide to the residue to neutralize to obtain disodium salt, then add 0.186 grams of catalyst ruthenium oxide, add 149.2 grams of 15% fresh sodium hypochlorite dropwise under stirring, control the temperature at about 50°C to complete the dropwise addition, and keep the temperature for 5 hours. After the oxidation reaction is basically completed, the catalyst is filtered out, most of the water is distilled off under negative pressure, then acetone is added, hydrogen chloride gas is introduced to ...

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Abstract

The invention relates to a method for synthesizing L-type glufosinate ammonium salt, which comprises the steps of reacting 4-(ethoxy-(methyl)phosphinyl)-2-acetoxybutane cyanide and hydrochloric acid to obtain 4-(hydroxy- (methyl) phosphinyl)-2-hydroxybutyric acid, then react with sodium hydroxide aqueous solution to obtain 4-(sodium hydroxy-(methyl) phosphinyl)-2-sodium hydroxybutyrate, and then react with sodium hypochlorite aqueous solution Obtain 4-(hydroxysodium-(methyl) phosphinyl)-2-sodium carbonyl butyrate, then react with hydrogen chloride gas to obtain 4-(hydroxy-(methyl) phosphinyl)-2-carbonyl butyric acid, then React with liquid ammonia, and then feed into hydrogen to react to obtain L-type glufosinate ammonium salt. The invention has the advantages of simple technological process, less pollution, high yield and low cost, and the finished product obtained by the invention is L-glufosinate-ammonium with high herbicidal effect, which greatly improves the herbicidal effect of glufosinate-ammonium.

Description

technical field [0001] The invention relates to a method for synthesizing L-type glufosinate-ammonium ammonium salt. Background technique [0002] As a phosphonic acid herbicide, glufosinate-ammonium is a partial systemic and non-conductive contact herbicide. By inhibiting the activity of glutamine synthetase in plants, it leads to the obstruction of glutamine synthesis, disorder of nitrogen metabolism, ammonia ion Accumulation, thereby destroying the plant cell membrane, preventing the plant from photosynthesizing and dying. With the increasing resistance to glyphosate, the increase of difficult-to-control weeds, and the approaching date of the ban on paraquat, glufosinate-ammonium, as an ideal substitute for large-tonnage weed control, has gradually become a hot spot in the industry. Except for the 90% L-type glufosinate-ammonium registered by Meiji Fruit Industry in Japan, all other companies sell a mixture of racemic DL-configuration, which greatly reduces the weeding e...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07F9/30
Inventor 闫立单顾松山余强蔡军义钱立东
Owner JIANGSU SEVENCONTINENT GREEN CHEM CO LTD
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