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

Method for synthesizing 2-(5-fluoro-2, 4 dinitro-phenoxy) acetate

A technology of dinitrophenoxy and dinitrobenzene, which is applied in the field of synthesizing 2-acetate, can solve the problems of severe nitration reaction conditions, easy breakage of ether bonds, and low product yield, so as to improve fluorination activity, High conversion rate and strong fluorination selectivity

Inactive Publication Date: 2019-05-14
内蒙古世杰化工有限公司
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] Among the various synthetic techniques that have been published so far, there are m-dichlorobenzene as raw materials, and the precursor 2-(5-fluoro-2,4-dinitrophenoxy) is obtained through nitration, fluorination, etherification and other steps. Acetate, when dichlorofluorinated to difluoro, the amount of tar is large, the product loss is large, etherification will produce impurities that both fluorines are etherified
There is 2,4-difluoronitrobenzene as the raw material, which undergoes hydrolysis, etherification, reduction, nitration, and reduction. Although the raw material is easy to obtain in this route, the route is long and the impurities are high. At the same time, hydrogenation is required twice, and the cost is increased. , cumbersome operation
There is m-fluorophenol as the starting material, although the reaction route is not very long, but the raw material is rare and expensive, the nitration reaction conditions are severe, the ether bond is easy to break, the impurities are high, and the product yield is low

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
  • Method for synthesizing 2-(5-fluoro-2, 4 dinitro-phenoxy) acetate
  • Method for synthesizing 2-(5-fluoro-2, 4 dinitro-phenoxy) acetate
  • Method for synthesizing 2-(5-fluoro-2, 4 dinitro-phenoxy) acetate

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0017] The following will clearly and completely describe the technical solutions in the embodiments of the present invention with reference to the accompanying drawings in the embodiments of the present invention. Obviously, the described embodiments are only some, not all, embodiments of the present invention. Based on the embodiments of the present invention, all other embodiments obtained by persons of ordinary skill in the art without making creative efforts belong to the protection scope of the present invention.

[0018] see figure 1 , a method for synthesizing 2-(5-fluoro-2,4-dinitrophenoxy) acetate, using 2,4-dichloro-1,5-dinitrobenzene as raw material through etherification and fluorination Reaction and workup give 2-(5-fluoro-2,4-dinitrophenoxy)acetate.

[0019] A further technical solution of the present invention comprises the following steps:

[0020] (1) etherification reaction

[0021] Put 500ml of DMF into a 1000ml reaction bottle, add 300g of 2,4-dichloro-...

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 method for synthesizing 2-(5-fluoro-2, 4 dinitro-phenoxy) acetate. 2, 4-dichloro-1, 5-dinitrobenzene serves as a raw material, the 2, 4-dichloro-1, 5-dinitrobenzene and hydroxy acetate are etherified in aprotic polar solvents DMF and react under the action of acid-binding agents and catalysts to obtain 2-(5-chlorine-2, 4 dinitro-phenoxy) acetate, and the 2-(5-chlorine-2,4 dinitro-phenoxy) acetate and potassium fluoride are fluoridated to obtain 2-(5-fluorine-2, 4-dinitro-phenoxy) acetate. Reaction raw materials in all steps are easy to obtain and economical, technological conditions are mild, a line is short, operation is simple and convenient, the method is high in safety and short in reaction time, and industrial production can be popularized.

Description

technical field [0001] The invention relates to the technical field of herbicide production and preparation, in particular to a method for synthesizing 2-(5-fluoro-2,4-dinitrophenoxy) acetate. Background technique [0002] 2-(5-fluoro-2,4-dinitrophenoxy) acetate is a kind of pesticide intermediate, which can synthesize the herbicide flumechlor, which is protoporphyrinogen oxidase ( PPO) inhibitors are used to control weeds and broad-leaved weeds on many crops such as soybeans, cotton, and grapes. The chemical structure of 2-(5-fluoro-2,4-dinitrophenoxy)acetate is as follows. Its chemical structural formula is as follows: [0003] [0004] Among the various synthetic techniques that have been published so far, m-dichlorobenzene is used as a raw material, and the precursor 2-(5-fluoro-2,4-dinitrophenoxy) is obtained through nitration, fluorination, etherification and other steps. When acetic ester is fluorinated from dichloro to difluoro, the amount of tar is large and th...

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 Applications(China)
IPC IPC(8): C07C201/12C07C205/37
Inventor 不公告发明人
Owner 内蒙古世杰化工有限公司
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