Magenta dyes and their preparation methods and applications

Patent metadata

Field	Value
Publication number	US-9011589-B2
Application number	US-201414216906-A
Country	US
Kind code	B2
Filing date	Mar 17, 2014
Priority date	Mar 20, 2012
Publication date	Apr 21, 2015
Grant date	Apr 21, 2015

Abstract

The present invention relates to a class of magenta dyes, their preparation methods and applications. The magenta dyes include the compounds which simultaneously contain carboxyl group, sulfonic acid group and the carbonyl propyl sulfurylsulfonic acid on the anthrapyridone skeleton, showing in the form of general formula (I) or their mixtures. In the general formula (I): A may be cation M 4 , or substituted or unsubstituted benzyl group, or substituted or unsubstituted naphthyl methyl; M 1 , M 2 , M 3 are respectively cation or cationic groups; Sulfonic acid group (SO 3 M 2 ) m may located any position of the benzene ring, of which m is an integer of 0-2. As containing carboxyl (or carboxylic benzyl ester or naphthoate), sulfonic acid groups and carbonyl propyl sulfuryl simultaneously, the magenta dyes of the present invention feature outstanding tone, brightness, light resistance, water resistance, ozone resistance as well as solubility and solution stability, etc.

First claim

What is claimed is:

1. A class of magenta dyes, include the compounds which simultaneously contain carboxyl group, sulfonic acid group and a carbonyl propyl sulfurylsulfonic acid group on an anthrapyridone skeleton, showing in the form of general formula (I) or their mixtures:

wherein in the general formula (I): A is a cation M 4 , a substituted or unsubstituted benzyl group, or a substituted or unsubstituted naphthyl methyl; M 1 , M 2 , M 3 are respectively cation or cationic groups; sulfonic acid group (SO 3 M2) m may be located any position of the benzene ring, and m is an integer of 0-2.

2. The magenta dyes according to claim 1 , wherein,
when A is cation M 4 , the general formula (I) is changed to the general formula (I′):

when A is substituted or unsubstituted benzyl group, the general formula (I) is changed to the general formula (II):

when A is substituted or unsubstituted naphthyl methyl, the general formula (I) is changed to the general formula (II′):

wherein in the general formula (II) and (II′), R 1 is H, C 1-6 alkyl group, CN, NO 2 , SO 3 H or SO 3 M 5 , F, Cl, Br, CO 2 H, CO 2 M 6 , CO 2 R 2 , or NHCOR 3 ; R 2 is H or C 1-6 alkyl group; R 3 is H or C 1-6 alkyl group; (R 1 )n may be located any position of the benzene ring, and n is an integer of 0-3;
in the general formula (I′), (II) and (II′), M 1 , M 2 , M 3 , M 4 , M 5 , M 6 are respectively cation or cationic groups; sulfonic acid group (SO 3 M 2 ) m may be located any position of the benzene ring, and m is an integer of 0-2.

3. The magenta dyes according to claim 2 , wherein M 1 , M 2 , M 3 , M 4 , M 5 , M 6 are selected from the group consisting of the following cation: H + , Li + , Na + , K + , NH 4 + and organic ammonium salts N + R 4 R 5 R 6 R 7 , of which R 4 , R 5 , R 6 , R 7 are respectively the same or different H, C 1-18 alkyl group, cyclohexyl group, CH 2 CH 2 OH, CH(CH 3 )CH 2 OH or benzyl group.

4. The magenta dyes according to claim 2 , wherein m is an integer of 1-2.

5. The magenta dyes according to claim 3 , wherein the organic ammonium salt N + R 4 R 5 R 6 R 7 is selected from the group consisting of:
monoethanolamine salt, diethanolamine salt, triethanolamine salt, monoisopropanolamine salt, diisopropanolamine salt and triisopropanolamine salt.

6. The magenta dyes according to claim 3 , wherein the cation is selected from the group consisting of H + , Li + , Na + , K + , and NH 4 + .

7. The magenta dyes according to claim 1 , wherein the compound shown in the general formula (I) may be utilized in the form of mixture with any weight ratio.

8. The magenta dyes according to claim 3 , wherein the compound shown in the general formula (I) may be utilized in the form of mixture with any weight ratio.

9. A method for preparing the compounds shown in the general formula (I) or their mixtures according to claim 1 , comprising the following steps:
(1) synthesizing an intermediate compound shown in the general formula (IV):

wherein in the general formula (IV), R 8 is C 1 -C 4 alkyl group;
cyclization steps comprise: based on a compound shown in general formula (III) or (III′) as a raw material, carrying out cyclization reaction on compound shown in the general formula (III) or (III′) and malonic acid diester (R 8 OOC—C—COOR 8 ) in an organic solvent at the temperature of 100° C-250° C. for 2-10 h to form the intermediate compound shown in the general formula (IV);

cool the reaction system after the cyclization and filter the compound of general formula (IV) separated out from the liquid reaction system to obtain solid intermediate (IV) compounds;
(2) sulfonation and decomposition step: the intermediate compound shown in the general formula (IV) is sulfonated with fuming sulfuric acid (SO 3 .H 2 SO 4 ) containing 5-30% SO 3 or chlorosulfonic acid under the temperature of 10° C-120° C., and simultaneously decomposition reaction is carried out for 2-4 h to obtain a sulfonation liquid; said sulfonation liquid comprises one or more sulfonation compounds shown in general formulas (V), (VI),(VII);

(3) hydrolysis step: the sulfonation compounds obtained in the step (2) are hydrolyzed at acid condition or alkaline condition;
hydrolysis at acid condition: heated the sulfonation liquid obtained in the step (2) to 40° C-80° C., and hydrolysis 1.5-5 h; then neutralizing the sulfuric acid in the sulfonation liquid utilizing alkali, finally obtained solution of a compound shown in general formula (I′),

hydrolysis at alkaline condition: neutralized the sulfonation liquid obtained in the step (2) utilizing alkali to neutral, then adjusted pH utilizing alkali to 9-10 emerging alkalescence, then heated to 40° C-80° C., hydrolyzed 1.5-5 h, finally obtained solution of the compound shown in the general formula (I′);
(4) benzylation step: solution of compound shown in general formula (II) is obtained by benzylation reaction utilizing benzylation reagent and solution of the compound shown in the general formula (I′) in the step (3) , temperature of the benzylation reaction is 50° C-150° C., pH of the benzylation reaction is 0-12, mole rate of the compound shown in the general formula (I′):benzylation reagent of the benzylation reaction is 1:1-100, reaction time of the benzylation reaction is 1-120 h

 or
naphthyl methylation step: solution of compound shown in general formula (II′) is obtained by naphthyl methylation reaction utilizing naphthyl methylation reagent and solution of the compound shown in the general formula (I′) in the step (3), temperature of the naphthyl methylation reaction is 70° C-150° C., pH of the naphthyl methylation reaction is 0-12, mole rate of the compound shown in the general formula (I′): naphthyl methylation reagent of the benzylation methylation reaction is 1:1-20, reaction time of the naphthyl methylation reaction is 0.5-10 h,

(5) salting-out step: the solution of compound shown in general formula (II) or the solution of compound shown in general formula (II′) obtained in the step (4) is salted out with a salt to generate a salt mixture, wherein the salt mixture comprises one or more salts of the compounds shown in the general formula (I);
(6) separation step: the salts of the compounds shown in the general formula (I) are separated out from the salt mixture by adopting stepwise salting out, reversed phase ion-pair chromatography, and the obtained salts of the compounds are respectively desalinated to generate the compounds shown in the general formula (I).

10. A method for preparing the compounds shown in the general formula (I) or their mixtures accordi

Assignees

• Univ Dalian Tech
• Zhuhai Ninestar Man Co Ltd

Inventors

• Peng Xiaojun
• Li Shiyu
• Wu Jinhe
• Meng Fanming
• Zhang Rong
• Fan Jiangli
• Wang Feng
• Li Shaolei

Classifications

• C09D11/328

  characterised by dyes · CPC title

• C09B5/14 Primary

  Benz-azabenzanthrones (anthrapyridones) · CPC title

• C09D11/02

  Printing inks (C09D11/30 takes precedence) · CPC title