GB298518A - Process for the manufacture of polyazo dyestuffs - Google Patents

Process for the manufacture of polyazo dyestuffs

Info

Publication number
GB298518A
GB298518A GB1796727A GB1796727A GB298518A GB 298518 A GB298518 A GB 298518A GB 1796727 A GB1796727 A GB 1796727A GB 1796727 A GB1796727 A GB 1796727A GB 298518 A GB298518 A GB 298518A
Authority
GB
United Kingdom
Prior art keywords
acid
amino
sulphonic acid
sulphonic
naphthol
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
GB1796727A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie 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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB1796727A priority Critical patent/GB298518A/en
Publication of GB298518A publication Critical patent/GB298518A/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
    • C09B31/00Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
    • C09B31/16Trisazo dyes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

298,518. Carpmael, A., (I. G. Farbenindustrie Akt.-Ges.). July 6, 1927. Azo dyes.-Relates to the manufacture of tetrakisazo dyes of the type R<1> # R<2> # R<3> # R<4> # X and of octakisazo dyes of the type R<1># R<2> # R<3> # R<4> # Z # R' # R<3> # R<2> # R<1> in which R' is an aromatic amine, R<2> is a diazotizable middle component of the naphthalene series, R<3> is a derivative of a sulphonated or unsulphonated 1- naphthylamine, coupled in p-position to the amino group and containing a free or substituted hydroxy group, R<4> is a derivative of 2 :5 : 7- aminonaphtholsulphonic acid containing a diazotizable amino group in the heteronuclear side chain (or a derivative thereof substituted also in the 1-position), and X and Z are coupling components selected from the following :-methyl ketol or a substitution product thereof, a pyrazolone, a derivative of a #-ketoaldehyde, 1 : 3- dioxyquinoline, a sulphazone of the formula or salicylic acid or a derivative thereof capable of coupling. The disazo dyestuff R<1> # R<2> # R<3> is diazotized and coupled with R<4>, and one molecular proportion of the resulting trisazo dyestuff is diazotized and coupled with X or two molecular proportions are diazotized and coupled with Z. The products dye cotton from a neutral or alkaline bath in clear green shades fast to light. The following examples are specified. (1) R<1> is aniline or its homologues or substitution products including its 3-sulphonic acid, 2 : 4- or 2 :5-disulphonic acid, 3-chloro-6- sulphonic acid, or 4-nitro-2 : 5-disulphonic acid, and 2-amino-1-methoxybenzene-4-sulphonic acid, or 2-amino-5-sulphobenzoic acid; R<2> is 1-aminonaphthalene or its 6- or 7-sulphonic acid; R<3> is 1-amino-2-ethoxynaphthalene-6-sulphonic acid, 1- amino-2-met,hoxy (or 2:7-dimethoxy) naphthalene, 1-amino-2-naphthoxy-#-propionic acid, the glycollic acid ether of 1-amino-2 : 7-dioxynaphthalene, or the sulphonic ester of 1-amino-2-oxyethoxynaphthalene; R<4> is 2-(4<1>-aminobenzoyl) amino - 5 - naphthol-7-sulphonic (or 1 : 7 - disulphonic) acid, 2-(4<1> [or 3<1>]-aminobenzoyl)amino-1- chloro-5-naphthol-7-sulphonic acid, 2-(4<11>-aminobenzoyl - 4<1>-aminobenzoyl)amino-5-naphthol-7-sulphonic acid, or the isomeric 3<11>-amino-4<1>- (or 3<1>) amino compounds, 3<1>-aminophenyl-1- : 2-naphthimidazol-5-oxy-7-sulphonic acid, 4<1> (or 3<1>)- aminophenyl-1 : 2-naphthothiazol - 5 - oxy - 7 - sulphonic acid, or the corresponding triazol derivatives, 3-amino-y-2 (5-oxy-7-sulpho)naphthylbenzimidazol, or 4'- (or 3<1>)-aminophenyl-2(5-oxy-7- sulpho)naphthyl urea; and X is methyl ketol or its sulphonic acid, sulphazone, salicylic acid, ocresotinic acid, 1 : 3-dioxyquinoline, 1-phenyl-3- methyl (or carboxy)-5-pyrazolone, or 1(2<1>[or 3<1> or 4<1>]-carboxy)phenyl-3-methyl-5-pyrazolone. (2) R<1> is 2-aminonaphthalene-4 : 8-disulphonic acid; R<2> is 1-aminonaphthalene; R<3> is 1-amino-2- methoxynaphthalene-6-sulphonic acid; R<4> is 3<1>- aminophenyl-1 : 2-naphthimidazol-5 - oxy - 7 - sulphonic acid; and X or Z is 1-(4<1>-carboxy)phenyl- 3-methyl-5-pyrazolone, or another of the pyrazolones enumerated in Example 1, or the pyrazolone or dipyrazolone obtained from the hydrazine of aniline-2 (or 3 or 4)-sulphonic acid, benzidine, dehydrothiotoluidine sulphonic acid, 5- amino-salicylic acid, 3-amino-5-sulphosalicylic acid, or 2: 5: 7-aminonaphtholsulphonic acid, or the condensation product from p-aminobenzaldehyde (1 mol.) and o-cresotinic acid (2 mols.). (3) R' is aniline-2 : 4-disulphonic acid, R<2> is 1-aminona.phthalene, R<3> is 1-amino-2-acetoxynaphthalene- 7-sulphonic acid, 1-amino-5-oxy (or acetoxy) naphthalene or its 6-sulphonic acid, or 1-amino- 8-oxy (or acetoxy) naphthalene-6-sulphonic acid; R<4> is 2-(3<1>-aminobenzoylamino-5-naphthol-7-sulphonic acid; and X or Z is acetoacetanilide or its 4-carboxylic acid, acetoacet-2-toluidide, acetoacet- 2-chloranilide, acetoacet-4-anisidide, acetoacet-5- nitro-4-chloro-2-anisidide, di-(acetoacet)-toluidide, benzoyl .acetanilide, or another derivative of a #- ketoaldehyde such as 1 : 3-diketohydrindene. The acetyl group, if present in the trisazo dyestuff, is split off before the final coupling. 4-Nitraniline-2 5-disulphonic acid is cbtained by direct nitration of aniline-2 : 5-disulphonic acid. 1-Amino-2-naphthoxy-#-propionic acid is obtained by treating 2-naphthol with #-chloropropionic acid in presence of an agent for combining with acid, nitrating and reducing the nitro group. 1-Amino-2- : 7-dioxynaphtalene glycollin acid ether is obtained by treating 2 : 7-dioxynaphthalene (1 mol.) with chloracetic acid (2 mols.) in presence of an agent for combining with acid, nitrating, and reducing the nitro group. 1-Amino - 2 - oxyethoxynaphthalene sulphonic ester is obtained by nitration of the sulphonic ester of 2-oxyethoxynaphthalene, prepared as described in Specification 265,940, and reduction of the nitro group. 2-(4<1>[ or 3<1>]-Aminobenzoyl)amino - 1 - chloro-5- naphthol-1-sulphonic acid is obtained by treating 2-amino-1-chloro-5-naphthol-7-sulphonic acid with 4 (or 3)-nitrobenzoyl chloride in presence of an agent for combining with acid, and reducing the nitro group. 4- (or 3<1>)-Aminophenyl-2 (5-oxy-7-sulyho)naphthyl urea is obtained by condensing 4-(or 3)-nitro. phenylurea or 4 (or 3)-nitrophenylisocyanate with 2 : 5 : 7-acid, and reducing the nitro group. 1-Amino-2-methoxynaphthalene-6-sulphonic acid is obtained by methylating 2-naphthol-6-sulphonic acid by means of dimethyl sulphate or methyl chloride, nitrating, and reducing the nitro group. 1-Amino-5-acetoxynaphthalene, its 6-sulphonic acid, and 1-amino-8-acetoxynaphthalene - 6 - sulphonic acid are obtained by treating 1 : 5-aminonaphthol, its 6-sulphonic acid, and 1 : 8-aminonaphthol-6-sulphonic acid respectively with acetic anhydride in alkaline solution at a low temperature. Acetoacet-5-nitro-4-chloro - 2 - anisidide is obtained by heating 5-niti-o-4-chloro-2,-anisidine with acetoacetic ester either alcne or in an indifferent solvent.
GB1796727A 1927-07-06 1927-07-06 Process for the manufacture of polyazo dyestuffs Expired GB298518A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1796727A GB298518A (en) 1927-07-06 1927-07-06 Process for the manufacture of polyazo dyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1796727A GB298518A (en) 1927-07-06 1927-07-06 Process for the manufacture of polyazo dyestuffs

Publications (1)

Publication Number Publication Date
GB298518A true GB298518A (en) 1928-10-08

Family

ID=10104332

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1796727A Expired GB298518A (en) 1927-07-06 1927-07-06 Process for the manufacture of polyazo dyestuffs

Country Status (1)

Country Link
GB (1) GB298518A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2476261A (en) * 1946-04-11 1949-07-12 Ciba Ltd Process for the manufacture of asymmetrical polyazo-dyestuffs
US2476260A (en) * 1946-04-11 1949-07-12 Ciba Ltd Process for the manufacture of disazo-dyestuffs

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2476261A (en) * 1946-04-11 1949-07-12 Ciba Ltd Process for the manufacture of asymmetrical polyazo-dyestuffs
US2476260A (en) * 1946-04-11 1949-07-12 Ciba Ltd Process for the manufacture of disazo-dyestuffs

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