Preparation method of isoindolinone pigment

A technology of isoindolinone and pigments, which is applied in the field of preparation of isoindolinone pigments, can solve the problems of poor weather resistance, heavy pollution and high cost, and achieve the effects of cheap raw materials, high yield and high tinting strength

Active Publication Date: 2022-03-18
LILY GRP CO LTD
View PDF10 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] The present invention aims at the problems existing in the prior art, provides the preparation method of isoindolinone pigment, replaces the use of highly toxic substances in the prior art with the green reagent, overcomes low yield, high cost and pollution in the prior art at the same time Defects of heavy weight, pigment dispersibility, and poor weather resistance

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
  • Preparation method of isoindolinone pigment
  • Preparation method of isoindolinone pigment
  • Preparation method of isoindolinone pigment

Examples

Experimental program
Comparison scheme
Effect test

Example Embodiment

[0044] Example 1

[0045] Tetrachlorochemisodiphenimic anhydride was 250g, phosphorus phosphorus 182 g, and phosphorus 160g of extol. The chlorinated product was introduced in advance to the reactor of 245 g of ammonia water, and the reactor of 3 g of sodium hydroxide was 3 h. Next, the reaction was reacted for 2 hours at a pressure vessel at 120 ° C. Then cool the temperature, separated, 236.5 g of intermediate TCCBM, ie (1), HPLC detects 99.2%; excess of dimethyl carbonate recovery.

[0046] The 20 g of intermediate TCCBM was added to 88 mL of methanol, and the organic base was 11.5 g of stirring for half an hour, then the 3.6 g of phenylenediamine dissolved in advance was 2 hours at normal temperature, and the temperature was continued to 50 ° C for 1 hour, then transferred to The reaction was reacted in 80 ml of water for 0.5 hours, and the pH is adjusted to 5.5 with a small amount of acetic acid / methicate, cooling filtration, washing, the resulting filter cake is pulped into

Example Embodiment

[0051] Example 2

[0052] The intermediate TCCBM obtained by 20 g of Example 1 was added to 100 mL of methanol, and the organic base was 12.1 g and stirred for half an hour, and then the 3.55 g of phenylenediamine dissolved in advance was 1 hour at 45 ° C, then warmed to 70 ° C. 1.5-2 hours, then transferred to 80 ml of water to react for 1 hour, adjusting the pH to 6.0 with a small amount of formic acid / hydrochloric acid, cooling filtration, washing, pulling the resulting filter cake, 0.5 g of alkyl naphthalenesulfonic acid, at 50-80 The reaction was reacted for 2 hours, then filtered, washed, dried.

Example Embodiment

[0053] Example 3

[0054] The intermediate TcCBM obtained by 20 g of Example 1 was added to 90 mL of methanol, and the organic base was 12.0 g of stirring for half an hour, then 4.05 g 2,6-dicharobenzene is reacted at room temperature for 0.5 hours, then warmed to 45 At ° C, the reaction was 1 hour, and finally heated to reflux continued to react for 1-2 hours, and finally transferred to 75 ml of water for 1 hour, and the pH is adjusted to 5.5 with a small amount of acetic acid / sulfate, and the filtered, washed, and the resulting filter cake was pulled. 0.4 g of quaternary ammonium salts were added, and the reaction was reacted at 30-60 ° C for 2 hours, then filtered, washed, dried, and finally green yellow pigment PY 109, 21.9 g.

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 present invention provides an isoindolinone pigment preparation method, and relates to the field of organic pigment preparation, the preparation method specifically comprises: carrying out a chlorination reaction on tetrachlorophthalic anhydride in a phosphorus oxychloride solvent, and carrying out an ammonolysis reaction and a methylation reaction under the action of a catalyst to generate an important intermediate TCCBM; then carrying out condensation reaction on the synthesized intermediate and a diamine compound in an alcohol solvent, then carrying out hydrolytic acidification reaction, filtering, washing with water, and pigmenting to obtain a target product. Compared with an existing technology for preparing similar isoindolinone, the raw materials used in the preparation method are easy to obtain; the methylation reagent is non-toxic, the solvent can be recycled and reused, and no pollution is caused to the environment; meanwhile, the reaction yield is increased, and the pigment is easy to disperse and weather-resistant.

Description

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

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
Owner LILY GRP CO LTD
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