GB918366A - Azo dyestuffs - Google Patents

Azo dyestuffs

Info

Publication number
GB918366A
GB918366A GB1321361A GB1321361A GB918366A GB 918366 A GB918366 A GB 918366A GB 1321361 A GB1321361 A GB 1321361A GB 1321361 A GB1321361 A GB 1321361A GB 918366 A GB918366 A GB 918366A
Authority
GB
United Kingdom
Prior art keywords
phenyl
general formula
radical
carbocyclic aryl
methyl
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
GB1321361A
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.)
Bayer AG
Original Assignee
Bayer 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 Bayer AG filed Critical Bayer AG
Publication of GB918366A publication Critical patent/GB918366A/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
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/24Monoazo dyes prepared by diazotising and coupling from coupling components containing both hydroxyl and amino directing groups
    • C09B29/28Amino naphthols
    • C09B29/30Amino naphtholsulfonic acid
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/02General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using azo dyes

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

2-Amino-benzene-sulphonic acid-N-phenyl-N-benzenesulphonyl imide is obtained by reacting 2-nitrobenzene sulphonic acid anilide with benzene sulphonic acid chloride and subjecting the product to catalytic hydrogenation. The product is used in azo dye preparation (see Group IV(c)).ALSO:The invention comprises azo dyestuffs of the general formula <FORM:0918366/IV (b)/1> wherein R denotes a radical of the benzene series to which the substituent -SO2- and -N=N- are linked ortho with respect to one another, X denotes a carbocyclic aryl or cycloalkyl radical, Y is a carbocyclic aryl radical and Z a hydrogen atom or an alkyl, carbocyclic aryl or aralkyl radical and the salts thereof and a process for the production thereof wherein the diazonium compound obtained by the diazotisation of an aromatic amine of the general formula <FORM:0918366/IV (b)/2> in which R, X and Y have the same meanings as above is coupled in an acid medium with a compound of the general formula <FORM:0918366/IV (b)/3> wherein 2 has the same meaning as above. The components specified in examples yield compounds of the first general formula above in which Y is phenyl, unsubstituted or substituted with a chlorine atom, a methyl group or -NHCOCH2Cl, X is phenyl, unsubstituted or substituted with one or two chlorine atoms, or a methyl, isopropyl, phenoxy or phenyl sulphonic group and Z is hydrogen, methyl, butyl or phenyl. The coupling is preferably carried out in aqueous acetic acid solution or suspension. Organic solvents such as formamide and dimethyl formamide may also be used. The products are red to bluish-red dyestuffs suitable for dying wool and polyamide fibres from an acid bath.
GB1321361A 1960-04-16 1961-04-12 Azo dyestuffs Expired GB918366A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF31027A DE1154890B (en) 1960-04-16 1960-04-16 Process for the production of azo dyes

Publications (1)

Publication Number Publication Date
GB918366A true GB918366A (en) 1963-02-13

Family

ID=7094021

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1321361A Expired GB918366A (en) 1960-04-16 1961-04-12 Azo dyestuffs

Country Status (4)

Country Link
BE (1) BE602632A (en)
CH (1) CH382337A (en)
DE (1) DE1154890B (en)
GB (1) GB918366A (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE964974C (en) * 1955-08-20 1957-05-29 Bayer Ag Process for the preparation of mono- and disazo dyes

Also Published As

Publication number Publication date
BE602632A (en) 1961-07-31
DE1154890B (en) 1963-09-26
CH382337A (en) 1964-09-30

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