GB949316A - New polyazo dyestuffs - Google Patents

New polyazo dyestuffs

Info

Publication number
GB949316A
GB949316A GB2456160A GB2456160A GB949316A GB 949316 A GB949316 A GB 949316A GB 2456160 A GB2456160 A GB 2456160A GB 2456160 A GB2456160 A GB 2456160A GB 949316 A GB949316 A GB 949316A
Authority
GB
United Kingdom
Prior art keywords
naphthol
amino
acid
group
formula
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
GB2456160A
Inventor
Frank Lodge
Cecil Vivian Stead
Cyril Eric Vellins
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB2456160A priority Critical patent/GB949316A/en
Publication of GB949316A publication Critical patent/GB949316A/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
    • C09B43/00Preparation of azo dyes from other azo compounds
    • C09B43/18Preparation of azo dyes from other azo compounds by acylation of hydroxyl group or of mercapto group
    • C09B43/26Preparation of azo dyes from other azo compounds by acylation of hydroxyl group or of mercapto group with polyfunctional acylating agents
    • C09B43/263Polycarboxylic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

Di -b - (3-amino -4- methoxyphenyl sulphonylethyl) terephthalate is obtained by reacting terephthaloyl chloride with 2-nitroanisole -4-b -hydroxy-ethyl sulphone and reducing the product with hydrogen in the presence of Raney nickel. The corresponding oxalate, fumarate and succinate are prepared by similar methods.ALSO:The invention comprises azo dyes of the formula <FORM:0949316/C3/1> wherein A and A1 each represent substituted or unsubstituted alkylene radicals containing from 2 to 6 carbon atoms and may be the same or different; D and D1 each represent the residue of an azo dye molecule and may be the same or different, T and T1, which are directly attached to carbon atoms present in D and D1 each represent a -SO2- or SO2 <FORM:0949316/C3/2> group and may be the same or different; R represents a hydrogen atom or a substituted or unsubstituted hydrocarbon radical and Z represents a direct link or a divalent hydrocarbon radical which may contain substituents and process for the preparation thereof wherein (a) two molecular proportions of a dyestuff of the formula D-T-A-OH or one molecular proportion of a dyestuff of the formula D-T-OH and one molecular proportion of a different dyestuff of the formula D1-T1-A1-OH wherein A, A1, D, D1, T and T1 have the meanings stated above are reacted with one molecular proportion of a halide of an acid of the formula <FORM:0949316/C3/3> wherein Z has the meaning given above or (b) an aromatic diamine which contains the group <FORM:0949316/C3/4> is tetrazotized and the tetrazo compound is coupled with 2 molecular proportions of a coupling component, or which 2 molecular proportions of an aromatic amine is diazotized and the diazo compound is coupled with one molecular proportion of a coupling component which contains the group <FORM:0949316/C3/5> where A, A1, T, T1 and Z have the meanings stated above. The carbon atom to which each of the groups T and T1 is linked may form part of an aryl radical present in the dye molecule or may form part of an alkyl chain directly attached to such an aryl radical or may be attached to an aryl radical through a group such as -O-, -S-, -NH-, <FORM:0949316/C3/6> alkyl -CO-and-CONH-. The radicals D and D1 may be the residues of mono- or polyazo dyes optionally containing a water solubilizing group, e.g. a carboxylic acid, alkyl sulphone, sulphamyl or sulphonic group and may also contain co-ordinately bound metal, e.g. copper, chromium or cobalt. Examples relate to the preparation of dyes by coupling diazotized di - b - (3 - amino - 4 - methoxyphenylsulphonylethyl) acid, 2-naphthol-3,6-disulphonic acid, 1 - (21 - chloro - 41 - sulpho - 61 - methylphenyl)-3 - methyl - 5 - pyrazolone, 2 - acetyl - amino-5 - naphthol - 7 - sulphonic acid, 1 - naphthol-5-sulphonic acid and 1-amino-8-naphthol-3,6-disulphonic acid (1-6); 3-amino-4-methoxyphenyl - b - hydroxyethyl - sulphone with 2-naphthol-6-sulphonic acid and condensing with terephtholoyl chloride (7); or isophthaloyl chloride (8); or by reacting the copper complex of 2 - (21 - hydroxy - 51 - b - hydroxyethyl-sulphonylphenylazo) - 1 - naphthol - 4 - sulphonic acid with terephthaloyl chloride (9); terephthaloyl chloride with [31-(b -hydroxyethylsulphonyl)phenyl] - 3 - methyl - 4 - (611-sulphonaphth - 211 - ylazo) - 5 - pyrazolone (10); or with 2 - [41 - (N - b - hydroxyethylsulphamyl) phenylazo] - 1 - naphthol - 4 - sulphonic acid (11); and by coupling di-b -(3-amino-4-methoxyphenylsulphonylethyl)oxalate, succinate and fumarate with 2-naphthol-3,6-disulphonic acid (12-13) and di-b -(3-amino-4-chlorophenylsulphonyl - ethyl)terephthalate with 2 - naphthol-6-sulphonic acid. The dyes are particularly suitable for colouring cellulose textile materials.
GB2456160A 1960-07-14 1960-07-14 New polyazo dyestuffs Expired GB949316A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2456160A GB949316A (en) 1960-07-14 1960-07-14 New polyazo dyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2456160A GB949316A (en) 1960-07-14 1960-07-14 New polyazo dyestuffs

Publications (1)

Publication Number Publication Date
GB949316A true GB949316A (en) 1964-02-12

Family

ID=10213569

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2456160A Expired GB949316A (en) 1960-07-14 1960-07-14 New polyazo dyestuffs

Country Status (1)

Country Link
GB (1) GB949316A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000069974A1 (en) * 1999-05-19 2000-11-23 The Procter & Gamble Company Reactive dye compounds
US6713613B1 (en) 1999-05-19 2004-03-30 North Carolina State University Reactive dye compounds
US6716969B1 (en) 1999-05-19 2004-04-06 North Carolina State University Reactive dye compounds
US6723834B1 (en) 1999-10-01 2004-04-20 North Carolina State University Reactive dye compounds
US6736864B1 (en) 1999-10-01 2004-05-18 North Carolina State University Reactive dye compounds
US6790943B1 (en) 1999-10-01 2004-09-14 North Carolina State University Reactive dye compounds
US6869453B1 (en) 1999-10-01 2005-03-22 North Carolina State University Reactive dye compounds
CN102344691A (en) * 2010-06-28 2012-02-08 住友化学株式会社 Dyes and colored compositions

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000069974A1 (en) * 1999-05-19 2000-11-23 The Procter & Gamble Company Reactive dye compounds
US6713613B1 (en) 1999-05-19 2004-03-30 North Carolina State University Reactive dye compounds
US6716969B1 (en) 1999-05-19 2004-04-06 North Carolina State University Reactive dye compounds
US6723834B1 (en) 1999-10-01 2004-04-20 North Carolina State University Reactive dye compounds
US6736864B1 (en) 1999-10-01 2004-05-18 North Carolina State University Reactive dye compounds
US6790943B1 (en) 1999-10-01 2004-09-14 North Carolina State University Reactive dye compounds
US6869453B1 (en) 1999-10-01 2005-03-22 North Carolina State University Reactive dye compounds
CN102344691A (en) * 2010-06-28 2012-02-08 住友化学株式会社 Dyes and colored compositions
CN102344691B (en) * 2010-06-28 2015-11-25 住友化学株式会社 Dye well coloured composition

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