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

Method for synthesizing aromatic amine

A technology of aromatic amine and aromatic trifluoromethanesulfonate, which is applied in the field of synthesizing aromatic amine, can solve the problems of poor stability, cumbersome operation, and long reaction time, and achieve mild reaction conditions, wide application range, and short reaction time. Effect

Inactive Publication Date: 2011-06-15
BEIJING INSTITUTE OF TECHNOLOGYGY
View PDF1 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In summary, in the known synthetic methods of aromatic amines, either the temperature is higher, or the reaction time is longer, or the required reagents are expensive, difficult to preserve, poor in stability, and cumbersome to use and operate.
These deficiencies have brought a lot of inconvenience to the synthesis of this type of compound, especially industrialized production

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 aromatic amine
  • Method for synthesizing aromatic amine
  • Method for synthesizing aromatic amine

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

Embodiment 2

Embodiment 3

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 provides a method for synthesizing aromatic amine. A reaction formula is shown in the specifications, wherein when X is nitrogen, a substituent group R can be 3- / 5-nitro, 3- / 5-cyan, 3- / 5-trifluoromethyl or 3- / 5-halo (fluorine, chlorine, bromine or iodine); when X is carbon, R can be 2- / 4-nitro, 2- / 4-cyan, 2- / 4-trifluoromethyl or 2-nitro-4-chlorine; R1 and R2 refer to hydrogen, alkyl, alkyl alcohol, benzyl or-(CH2)n-(n=2-6) naphthenic base respectively; reaction alkali is caesium carbonate, potassium phosphate, pyridine, triethylamine, sodium bicarbonate, potassium carbonate, sodium / potassium hydroxide or sodium / potassium alkoxide; a reaction solvent is dioxane, toluol, dimethyl sulfoxide, dimethyl formamide, acetonitrile, tetrahydrofuran or acetone; and the reaction is implemented in the conventional heating state. In the method, raw materials are readily available, the process is simple, the reaction condition is mild, the application range is wide, and a plurality of aromatic amine compounds can be synthesized by different substrates.

Description

A kind of method of synthesizing aromatic amine (1) Technical field The invention relates to a synthesis method for preparing aromatic amine (arylamine in English) through the reaction of aromatic trifluoromethanesulfonate and zinc chloride complex of secondary amine. (2) Background technology Aromatic amine compounds are extremely important organic raw materials, widely used in the production of dyes, medicines, agricultural chemicals, additives, surfactants, textile auxiliaries, chelating agents, polymers, flame retardants, etc. (Catal.Commun., 2007, 8, 629). For example, p-nitrodimethylaniline (p-NDMA) can be used for the determination of sliding arc discharge degradation methyl violet (Journal of Zhejiang University <Engineering Science Edition>, 2009, 43, 931); RT base (N-phenyl-1 , 4-phenylenediamine) is an important intermediate for the production of various rubber antioxidants with excellent properties (Journal of Nanjing Institute of Chemical Technology, 19...

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): C07B43/04C07D295/073C07D213/74C07D213/73C07C209/18C07C211/52C07C215/16C07C213/02
Inventor 李加荣徐娟史大昕张奇
Owner BEIJING INSTITUTE OF TECHNOLOGYGY
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