GB643054A - Process for the preparation of dis- and polyazo dyestuffs - Google Patents

Process for the preparation of dis- and polyazo dyestuffs

Info

Publication number
GB643054A
GB643054A GB1309/48A GB130948A GB643054A GB 643054 A GB643054 A GB 643054A GB 1309/48 A GB1309/48 A GB 1309/48A GB 130948 A GB130948 A GB 130948A GB 643054 A GB643054 A GB 643054A
Authority
GB
United Kingdom
Prior art keywords
acid
coupling
hydrogen
dyestuff
diazotized
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
GB1309/48A
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 GB643054A publication Critical patent/GB643054A/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
    • C09B39/00Other azo dyes prepared by diazotising and coupling

Landscapes

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

Abstract

A compound which is probably 1 : 2 : 7-triamino-8-naphthol-6-sulphonic acid is produced by reduction, with stannous chloride and hydrochloric acid, of the disazo dyestuff obtained by coupling diazotized 2-amino-5-nitrobenzene-1-sulphonic acid with 2 : 8 : 6-aminonaphtholsulphonic acid in an acid medium, acetylating the resulting monoazo dyestuff and coupling the product with diazotized a -naphthylamine in an alkaline medium.ALSO:Dis- and poly-azo dyestuffs are manufactured by coupling diazo compounds with azo dyestuffs of the general formula <FORM:0643054/IV (c)/1> wherein R represents the residue of a diazo compound and X hydrogen or SO3H, and wherein Y1 represents <FORM:0643054/IV (c)/2> (R1 being hydrogen, alkyl, cycloalkyl, aralkyl or aryl) and Y2 hydrogen, or vice versa when X is hydrogen, and, if desired, treating the product with a saponifying agent (e.g. sodium carbonate, ammonia, barium hydroxide, caustic soda solution, acetic acid or mineral acids), at ordinary or increased temperatures, in order to convert the <FORM:0643054/IV (c)/3> group into NHR1. The coupling, which takes place in the 7-position, and in positions capable of coupling in R when such are present, may be effected in the presence of acid binding agents, e.g. sodium acetate, sodium bicarbonate, potassium carbonate, caustic soda solution, calcium hydroxide, ammonia or tertiary organic bases such as pyridine. The starting materials are obtainable by the process of Specification 643,046, and the acyl groups specified correspond to the acylating agents therein enumerated, with the exception of thiophosgene chlorsulphonic acid and thioacetic acid, but with the addition of succinic acid. Examples and a table illustrate the use of a variety of diazo compounds, including diazotized aminoazo and aminodisazo dyestuffs, tetrazotized diamines, and the diazoazo compounds obtained from the latter by coupling with an equimolecular proportion of a coupling component. The products dye animal, vegetable or synthetic fibres or leather, and, if they contain groups capable of forming complexes, may be treated in substance or on the fibre with metal-yielding agents. Reference is also made to the diazotization and coupling on the fibre of the aminotrisazo dyestuff obtained by saponification of the dyestuff 2 - naphthylamine - 5 - sulphonic acid-->(acid) 1 : 5 : 7 - aminonaphtholsulphonic acid (acetylated) (alkaline)\sMbenzidine-->salicylic acid. Specification 281,410, [Class 15 (ii)], also is referred to. The Specification as open to inspection under Sect. 91 comprises also the use of coupling components in which R1 in the grouping <FORM:0643054/IV (c)/4> represents a second acyl group. This subject-matter does not appear in the Specification as accepted.
GB1309/48A 1947-01-17 1948-01-15 Process for the preparation of dis- and polyazo dyestuffs Expired GB643054A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH643054X 1947-01-17

Publications (1)

Publication Number Publication Date
GB643054A true GB643054A (en) 1950-09-15

Family

ID=4525573

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1309/48A Expired GB643054A (en) 1947-01-17 1948-01-15 Process for the preparation of dis- and polyazo dyestuffs

Country Status (1)

Country Link
GB (1) GB643054A (en)

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