GB766015A - Improvements in or relating to disazo dyestuffs - Google Patents

Improvements in or relating to disazo dyestuffs

Info

Publication number
GB766015A
GB766015A GB19904/54A GB1990454A GB766015A GB 766015 A GB766015 A GB 766015A GB 19904/54 A GB19904/54 A GB 19904/54A GB 1990454 A GB1990454 A GB 1990454A GB 766015 A GB766015 A GB 766015A
Authority
GB
United Kingdom
Prior art keywords
amino
aniline
mol
acid
anilines
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
Application number
GB19904/54A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sandoz AG
Original Assignee
Sandoz AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sandoz AG filed Critical Sandoz AG
Publication of GB766015A publication Critical patent/GB766015A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B62/00Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/02Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
    • C09B62/04Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to a triazine ring
    • C09B62/08Azo dyes
    • C09B62/09Disazo or polyazo dyes
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B31/00Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
    • C09B31/02Disazo dyes
    • C09B31/08Disazo dyes from a coupling component "C" containing directive hydroxyl and amino groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

The invention comprises dyestuffs of formula <FORM:0766015/IV(b)/1> where R is a benzene residue containing a water-solubilizing group and X is halogen, OH, NH2 or the residue of a primary or secondary amine. They are made by condensing 1 mol of a triazine compound which contains 3 replaceable halogen atoms bound to carbon atoms, e.g. cyanuric trichloride, with 1 mol of the aminodisazo compound made by diazotising 4-amino-1, 11-azobenzene- 3, 41-disulphonic acid and coupling in the 6 position of 2-amino-5-naphthol-7-sulphonic acid and with 1 mol of an appropriate aniline derivative and, if desired, with 1 mol of ammonia or a primary or secondary amine, the condensing operations being effected in any desired sequence. Alternatively they may be made by coupling diazotised 4-amino-1, 11-azobenzene-3, 41-disulphonic acid with a compound of formula <FORM:0766015/IV(b)/2> where R and X are as above and if X is halogen it may be replaced as before. Specified water-solubilizing groups are SO3 H, COOH, SO2NH2 which may be N-substituted and alkylsulphonyl groups. Condensations are advantageously effected in an aqueous medium in the presence of an acid-binding agent such as lithium sodium or potassium hydroxides, carbonates, bicarbonates and acetates. Where the water-solubility of the aniline derivative is slight it may be added in a solvent such as acetone. The aminodisazo compound is made by coupling diazotized 4-amino-1, 11-azobenzene-3, 41-disulphonic acid with a 2-acylamino-5-naphthol-7-sulphonic acid in neutral to weakly acid medium, separating the byproduct coupled in the 8-position, and saponifying the acylamino group in the derived intermediate dyestuff. The triazine used in the second modification is made by condensing 1 mol of an appropriate triazine compound which contains three halogen atoms with 1 mol of 2-amino- 5-naphthol-7-sulphonic acid and 1 mol of the required aniline derivative and, if desired, replacing a third halogen atom, if present by an appropriate amine or OH residue. Preferred anilines are aniline-3- and 4-sulphonic acids, -sulphononamides and carboxylic acids and 1-amino-3- and 4-methylsulphonylbenzenes. The anilines may contain further substituents e.g. halogen atoms and alkyl groups. Primary or secondary amines used may contain substituents such as halogen atoms or hydroxyl groups, and they may be aliphatic carbocyclic or heterocyclic, those specified being the above anilines and methyl-, dimethyl-, ethyl-, 2-hydroxy-ethyl-, di-(2-hydroxyethyl)-, propyl-, 3-hydroxy-propyl-, butyl-, amyl-, hexyl-, benzyl-, and cyclohexyl-amines, morpholine, aniline, 3-and 4-chloro - and - methyl-anilines, 4-methoxy - and - acetylamino-anilines, 1-amino-dimethylbenzenes, N-methyl - and - ethyl - aniline and 1- and 2-napthylamine sulphonic acids. A preferred series of dyestuffs are those where R is the residue of an aniline sulphonic acid or sulphonamide and/or X is a residue of an aminobenzene. The dyestuffs dye cotton and regenerated cellulose films in scarlet to red shades. Examples are provided of the preparation of the dyestuffs and their use in dyeing cotton and regenerated cellulose fibres primary and secondary amines used apart from those specified above being octylamine, 4-ethylamine and aniline-3-sulphonic acid methylamide and additional compounds corresponding to R being aniline 3-dulphonic acid methyl-and dimethyl-amides and 4- (21hydroxy) -ethyl-and - (21-carboxy) - phenyl-amides and 1 - amino - 3 - phenyl - sulphonyl-benzene.
GB19904/54A 1953-07-09 1954-07-07 Improvements in or relating to disazo dyestuffs Expired GB766015A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH766015X 1953-07-09

Publications (1)

Publication Number Publication Date
GB766015A true GB766015A (en) 1957-01-16

Family

ID=4535043

Family Applications (1)

Application Number Title Priority Date Filing Date
GB19904/54A Expired GB766015A (en) 1953-07-09 1954-07-07 Improvements in or relating to disazo dyestuffs

Country Status (1)

Country Link
GB (1) GB766015A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0357915A1 (en) * 1988-07-30 1990-03-14 Bayer Ag Disazo dyes

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0357915A1 (en) * 1988-07-30 1990-03-14 Bayer Ag Disazo dyes

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