Method for synthesizing 1,3-diiminoisoindoline by using mixed solvent

A bis-imino and mixed solvent technology, applied in the direction of organic chemistry, can solve the problems of insufficient raw materials in the phthalonitrile method and unstable reactions in the solid phase melting method, and achieve solutions to unstable reactions, insufficient raw materials, and high yields. Improved effect

Inactive Publication Date: 2018-04-13
SHANDONG HUIHAI PHARMA & CHEM
View PDF3 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] The object of the present invention is to provide a method for synthesizing 1,3-bis-iminoisoindoline using a mixed solvent, which not only overcomes the shortage of raw materials in the phthalonitrile method, but also solves the problem of unstable reaction in the solid phase melting method

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 1,3-diiminoisoindoline by using mixed solvent

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] Add phthalic anhydride and urea into 2000L xylene and mix according to the molar ratio of 7:3, raise the temperature to 132°C and keep it warm for 0.5h. After the water is separated, start to evaporate the solvent. Cooling and suction filtration to obtain solid phthalimide;

[0023] Throw phthalimide, urea, ammonium nitrate, and ammonium molybdate into 2000L of dichlorobenzene at a molar ratio of 100:300:124:1, and heat up to above 150°C for 2 hours after the reaction. Evaporate the solvent, after the solvent is evaporated, cool down to below 110°C, add a certain amount of water, stir, cool down and suction filter to obtain the wet product nitrate;

[0024] Add a certain amount of water to the wet product nitrate and beat for more than 20 minutes. After beating, add liquid caustic soda with a mass fraction of 30% at room temperature. The mass ratio of wet product nitrate, water and liquid caustic soda is 13:15:12. Clear to the process of product precipitation, stir for...

Embodiment 2

[0026] Add phthalic anhydride and urea to 2000L of methanol according to the molar ratio of 5:3 and mix them. Raise the temperature to 132°C and keep it warm for 0.5h. After the water is separated, start to evaporate the solvent. Suction filtration obtains solid phthalimide;

[0027] Put phthalimide, urea, ammonium nitrate, and ammonium molybdate in a molar ratio of 100:300:124:1 into a mixed solvent of 2000L methyl acetate and ethanol, and heat up to above 150°C for reaction After 2 hours, evaporate the solvent after the reaction is completed. After the solvent is evaporated, cool down to below 110°C, add a certain amount of water, stir and cool down, and suction filter to obtain the wet product nitrate;

[0028] Add a certain amount of water to the wet product nitrate and beat for more than 20 minutes. After beating, add liquid caustic soda with a mass fraction of 30% at room temperature. The mass ratio of wet product nitrate, water and liquid caustic soda is 13:15:12. Clea...

Embodiment 3

[0030] Add phthalic anhydride and urea into the mixed solvent of 2000L ethyl acetate and benzene according to the molar ratio of 6:3 and mix evenly, raise the temperature to 132°C and keep it warm for 0.5h. After the water is separated, start to evaporate the solvent, and cool down after evaporation Add water to 100°C and stir, cool down and filter with suction to obtain solid phthalimide;

[0031] Put phthalimide, urea, ammonium nitrate, and ammonium molybdate in a molar ratio of 100:300:124:1 into a mixed solvent of 2000L toluene and methanol. After the reaction, the solvent is evaporated, and after the solvent is evaporated, the temperature is lowered to below 110°C, a certain amount of water is added, the temperature is stirred, the temperature is lowered and the suction is filtered, and the wet product nitrate is obtained;

[0032] Add a certain amount of water to the wet product nitrate and beat for more than 20 minutes. After beating, add liquid caustic soda with a mass...

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 1,3-diiminoisoindoline by using a mixed solvent. By using a solvent method in a synthesis method of phthalic anhydride to synthesize the 1,3-diiminoisoindoline, the disadvantage of raw material shortage of a phthalonitrile method and defect of unstable reaction in a solid-phase melting method are overcome. The method has the advantages of simple and easily-controlled process and safe operation; in addition, the yield of the 1,3-diiminoisoindoline reaches 90 percent or above.

Description

technical field [0001] The invention belongs to the technical field of chemical synthesis, and in particular relates to a method for synthesizing 1,3-bisiminoisoindoline using a mixed solvent. Background technique [0002] 1,3-Diiminoisoindoline (1,3-diiminoisoindoline) is an important intermediate in organic synthesis, mainly used in the synthesis of phthalocyanine and isoindoline organic pigments, phthalocyanine dyes, and can also be used In the synthesis of porphyrazine, react with 1,3,4-thiadiazole to form a heterocyclic ring system and use it as a ligand to synthesize metal complexes. [0003] At present, there are two main methods for the synthesis of 1,3-bis-iminoisoindoline: [0004] Route 1 phthalonitrile method: mix the raw material phthalonitrile with the catalyst, add it to the alcohol solvent in the reactor, stir, feed ammonia gas and raise the temperature to a certain temperature, and react at this temperature for a fixed time to obtain the reaction liquid . ...

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): C07D209/44
CPCC07D209/44
Inventor 王后斌孙成斌于西波张世凤张翠翠娄丽丽
Owner SHANDONG HUIHAI PHARMA & CHEM
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap