GB858181A - Improvements in the production of diazapolymethine dyestuffs - Google Patents
Improvements in the production of diazapolymethine dyestuffsInfo
- Publication number
- GB858181A GB858181A GB6009/58A GB600958A GB858181A GB 858181 A GB858181 A GB 858181A GB 6009/58 A GB6009/58 A GB 6009/58A GB 600958 A GB600958 A GB 600958A GB 858181 A GB858181 A GB 858181A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- dyestuffs
- salt
- thiadiazolone
- phenyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B27/00—Preparations in which the azo group is formed in any way other than by diazotising and coupling, e.g. oxidation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Abstract
The invention comprises diazapolymethine dyestuffs having cations of the general formula: <FORM:0858181/IV (c)/1> wherein R is an alkyl or aryl group, Y is a divalent heteroatom or -NH-, -N (alkyl)-, -N (aryl)-, or -N (NH2)-, X is a divalent azomethine group substituted on the carbon atom, and R1 is the residue of a coupling compound. The dyestuffs may be obtained by subjecting hydrazones of the formula: <FORM:0858181/IV (c)/2> wherein X, Y, and R have the meanings indicated above, to an oxidizing coupling reaction with coupling components in the presence of oxidizing or dehydrogenating agents. Hydrazones mentioned include those of 3- methyl -5- anilino-1. 3. 4- thiadiazolone-(2), 3- methyl -5- phenyl-1. 3. 4- oxadiazolone- (2), 1-methyl -3- phenyl-4- nbutyl -1. 2. 4- triazolone- (5), 1 -methyl -3-phenyl -4- amino -1. 2. 4- triazolone- (5), 2-methylmercapto -4- methyl -1. 3. 4- thiadiazolone-(5), and 3- methyl -5- (41- methoxy)- anilino-1. 3. 4- thiadiazolone- (2). As coupling components there may be used phenols, naphthols, enols, aromatic amines, or eneamines. The oxidizing or dehydrogenating agent may be a ferric or cupric salt, ferricyanide, mercury (II) salt, cerium (IV) salt, persulphate, perborate, hypochlorite, peroxide, oxygen or air. Yellow to greenish-blue dyes are obtained. Preferred coupling components are those containing an amino group e.g. an aromatic amine, or an indole derivative such as an alkyl or arylindole. The basic diazapolymethine dyestuffs are specially suitable for dyeing polyacrylonitrile fibres. In examples, 3- methyl -5- anilino -1. 3. 4- thiadiazolone -(2)- hydrazone -5- hydrochloride is coupled with dimethyl aniline in presence of ferric chloride to form a dyestuff salt of the formula: <FORM:0858181/IV (c)/3> 2- methylmercapto -4- methyl -1. 3. 4- thiadiazo-lone -(5)-hydrazone is coupled with 3- amino-toluene in presence of ferric chloride and the dye is precipitated with a solution of zinc and sodium chlorides to form a dye salt of formula: <FORM:0858181/IV (c)/4> Many other dyestuffs of the stated general formula are specified, including those in the production of which there are used as coupling components, naphthols, naphthol sulphonates, amino phenols, toluols, phenylene diamines, diphenylamines, ethoxy diphenylamines, toluidines, cyanoethyl anilines, hydroxyethyl anilines, phenyl pyrazolones, and acetoacetanilide. Specification 857,198 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE858181X | 1957-02-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB858181A true GB858181A (en) | 1961-01-11 |
Family
ID=6789768
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB6009/58A Expired GB858181A (en) | 1957-02-26 | 1958-02-25 | Improvements in the production of diazapolymethine dyestuffs |
Country Status (2)
Country | Link |
---|---|
FR (1) | FR1199411A (en) |
GB (1) | GB858181A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4818815A (en) * | 1985-07-26 | 1989-04-04 | Ciba-Geigy Corporation | Cationic 1,2,3-thiadiazole-azo-aniline or tetrahydroquinoline compounds |
US7497878B2 (en) | 2005-06-30 | 2009-03-03 | L'oreal, S.A. | Azo dyes containing a sulphonamide or amide function for the dyeing of human keratin fibers and method of dyeing and dyeing compositions containing them |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2811258C2 (en) * | 1978-03-15 | 1982-12-30 | Bayer Ag, 5090 Leverkusen | 1,3,4-thiadiazole cationic dyes, processes for their preparation and processes for dyeing and printing natural and synthetic materials |
DE4426941A1 (en) | 1994-07-29 | 1996-02-01 | Bayer Ag | Cationic 1,3,4-thiadiazole dyes |
DE4444863A1 (en) | 1994-12-16 | 1996-06-20 | Bayer Ag | Cationic 1,3,4-thiadiazole dyes |
-
1958
- 1958-02-25 GB GB6009/58A patent/GB858181A/en not_active Expired
- 1958-02-25 FR FR1199411D patent/FR1199411A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4818815A (en) * | 1985-07-26 | 1989-04-04 | Ciba-Geigy Corporation | Cationic 1,2,3-thiadiazole-azo-aniline or tetrahydroquinoline compounds |
US7497878B2 (en) | 2005-06-30 | 2009-03-03 | L'oreal, S.A. | Azo dyes containing a sulphonamide or amide function for the dyeing of human keratin fibers and method of dyeing and dyeing compositions containing them |
Also Published As
Publication number | Publication date |
---|---|
FR1199411A (en) | 1959-12-14 |
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