Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Production process of 4-(hydroxy-(methyl)phosphinyl)-2-oxobutanoic acid

A technology of oxobutyric acid and production process, which is applied in the field of preparation of organic compounds, can solve the problems of discounted weeding effect, difficult storage, easy copolymerization, etc., and achieve the effect of clean production process, low cost and high weeding effect

Inactive Publication Date: 2016-03-23
盐城联合伟业化工有限公司
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] 4-(Hydroxy-(methyl)phosphinyl)-2-oxobutyric acid is an important intermediate for the synthesis of glufosinate-ammonium herbicides. It has the disadvantages of difficult storage and easy copolymerization. The longer the storage time, the dimer In addition, the common glufosinate-ammonium on the market is mixed glufosinate-ammonium, and its effect as a herbicide has certain limitations, because the herbicide is left-handed glufosinate-ammonium, and the existing production process can obtain When the 4-(hydroxyl-(methyl)phosphinyl)-2-oxobutanoic acid is used for the synthesis of glufosinate-ammonium, all the glufosinate-ammonium is mixed, so its herbicidal effect is greatly reduced

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Production process of 4-(hydroxy-(methyl)phosphinyl)-2-oxobutanoic acid
  • Production process of 4-(hydroxy-(methyl)phosphinyl)-2-oxobutanoic acid
  • Production process of 4-(hydroxy-(methyl)phosphinyl)-2-oxobutanoic acid

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0061] reference Figure 1 to 6 , A process for producing 4-(hydroxy-(methyl)phosphinyl)-2-oxobutanoic acid, which sequentially includes the following steps:

[0062] (1) Synthesis of methyl phosphine dichloride: add quantitative phosphorus trichloride and aluminum trichloride to the complexing kettle in sequence, stir, heat up (heating by heat transfer oil) to 60℃, and pass in methyl chloride (methyl chloride evaporates) The hot water temperature of the heater is controlled at 40-50°C; the pressure of the methyl chloride buffer tank is about 0.2MPa), the reaction temperature in the complexing kettle is controlled at 70°C, the pressure is 0.2MPa, and the reaction is about 3 hours, stop feeding methyl chloride, and then heat to Keep the temperature at 130°C for 3 hours (control the kettle pressure 3 It is generated into hydrochloric acid and phosphorous acid in the water, and discharged from the exhaust cylinder after being neutralized by the alkali solution, and then transferred ...

Embodiment 2

[0092] reference Figure 1 to 6 , A production process of 4-(hydroxy-(methyl)phosphinyl)-2-oxobutanoic acid, which is different from Example 1 as follows:

[0093] (1) Synthesis of methyl phosphine dichloride: add quantitative phosphorus trichloride and aluminum trichloride to the complexing kettle in turn, stir, heat up (heating by heat transfer oil) to 50℃, and pass in methyl chloride (methyl chloride evaporates) The temperature of the hot water of the heater is controlled at 40-50℃; the pressure of the methyl chloride buffer tank is about 0.2MPa), the reaction temperature in the complexing kettle is controlled at 50℃, the pressure is 0.1MPa, and the reaction is about 5 hours, stop feeding methyl chloride, and then heat to Keep the temperature at 100°C for 3 hours (control the kettle pressure <0.3MPa); after the heat preservation, cool to below 60°C and release the pressure to normal pressure (the gas phase is discharged into the exhaust gas absorption device, and treated with ...

Embodiment 3

[0104] reference Figure 1 to 6 , A production process of 4-(hydroxy-(methyl)phosphinyl)-2-oxobutanoic acid, which is different from Example 1 as follows:

[0105] (1) Synthesis of methyl phosphine dichloride: add quantitative phosphorus trichloride and aluminum trichloride to the complexing kettle in sequence, stir, heat up (heating by heat transfer oil) to 20℃, and pass in methyl chloride (methyl chloride evaporates) The hot water temperature of the heater is controlled at 40-50°C; the pressure of the methyl chloride buffer tank is about 0.2MPa), the reaction temperature in the complexing kettle is controlled at 40°C, the pressure is 0.05MPa, and the reaction is about 8 hours, stop feeding methyl chloride, and then heat to At 60°C, heat preservation for 3 hours (control kettle pressure3 It is generated into hydrochloric acid and phosphorous acid in the water, and discharged from the exhaust cylinder after being neutralized by the alkali solution, and then transferred to the pho...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a preparation method of 4-(hydroxy-(methyl)phosphinyl)-2-oxobutyric acid. The preparation method comprises following steps: synthesis of methylphosphoric dichloride; recovery of diethyl phthalate, synthesis of methyl chloro phosphinic propionyl chloride; synthesis of methoxyl methyl phosphinic methyl propionate; synthesis of 4-(hydroxy-(methyl)phosphinyl)-2-oxobutyric acid; and post treatment. Technology processes of the preparation method are simple; yield is high; production cost is low; and production technology is clean. In addition, when 4-(hydroxy-(methyl)phosphinyl)-2-oxobutyric acid obtained by the preparation method is used for synthesis of weed killer glufosinate-ammonium, levo glufosinate-ammonium with high weed killing function is obtained, so that weed killing effect of glufosinate-ammonium is improved greatly.

Description

Technical field [0001] The invention relates to a preparation method of organic compounds, in particular to a production process of 4-(hydroxy-(methyl)phosphinyl)-2-oxobutyric acid. Background technique [0002] Glufosinate-ammonium, a phosphonic acid herbicide, is a glutamine synthesis inhibitor. It is a non-selective contact herbicide. It controls monocot and dicot weeds at 1~2kg / ha. It transfers in the leaves, but cannot transfer. Elsewhere, when glutamine synthesis is inhibited, ammonium ions accumulate and the photosynthetic layer is destroyed. This product can be used to control annual and perennial dicotyledons and gramineous weeds in orchards, vineyards, and non-arable land. [0003] 4-(Hydroxy-(methyl)phosphinyl)-2-oxobutyric acid is an important intermediate for the synthesis of glufosinate-ammonium herbicide. It has the disadvantages of difficult storage and easy copolymerization. The longer the storage time, the dimer The higher; in addition, the common glufosinate-am...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C07F9/30
Inventor 顾伟方陈孝君马一帆吕建平陆文明徐澄
Owner 盐城联合伟业化工有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com