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CH348762A - Process for the production of water-insoluble azo dyes - Google Patents

Process for the production of water-insoluble azo dyes

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Publication number
CH348762A
CH348762A CH348762DA CH348762A CH 348762 A CH348762 A CH 348762A CH 348762D A CH348762D A CH 348762DA CH 348762 A CH348762 A CH 348762A
Authority
CH
Switzerland
Prior art keywords
sep
oxy
naphthoylamino
benzene
green
Prior art date
Application number
Other languages
German (de)
Inventor
Herbert Dr Kracker
Hans Dr Albert
Original Assignee
Hoechst 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 Hoechst Ag filed Critical Hoechst Ag
Publication of CH348762A publication Critical patent/CH348762A/en

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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
    • C09B31/02Disazo dyes
    • C09B31/06Disazo dyes from a coupling component "C" containing a directive hydroxyl group

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Description

  

  Verfahren zur     Herstellung    von     wasserunlöslichen        Azofarbstoffen       Aus der deutschen     Patentschrift    Nr. 609334 ist  bekannt, wasserunlösliche     Dis.azofarbstoffe    dadurch  herzustellen, dass man     diazotierte        Substitutionspro-          dukte    des     2-Amino-1,1'-azobenzols    mit     Oxyarylcar-          bonsäurearyliden,

          ss-Ketocarbonsäureestern    und     -ary-          liden    oder Derivaten von     Pyrazolonen    für sich. oder  auf einer Grundlage kuppelt. Man erhält auf diese    Weise Farbstoffe, die auf der Faser im allgemeinen  braune Färbungen von guten Echtheitseigenschaften  ergeben.  



  Es wurde nun gefunden, dass man zu wertvollen  wasserunlöslichen     Azofarbstoffen    gelangt, wenn man  die     Diazoniumverbindungen    aus     o-Amino-azoverbin-          dungen    der Formel  
EMI0001.0020     
    worin X eine     Alkyl-    oder     Alkoxygruppe    bedeutet, mit       Arylamiden    der     2,3-Oxy-naphthoesäure,    die keine       wasserlöslichmachenden    Gruppen enthalten, kuppelt.  



  Mit den neuen Farbstoffen erhält man auf der  pflanzlichen Faser, einschliesslich solcher aus regene  rierter     Cellulose,    nach den bekannten Färbeverfah  ren     grünstichigbraune    bis grüne Färbungen von guten  Echtheitseigenschaften, wie sie bisher in der     Eisfar-          benreihe    unter Verwendung geeigneter     Diazokompo-          nenten    noch nicht erhalten werden konnten.  



  Die Farbstoffe lassen sich in Substanz oder auf  einem nicht textilen Substrat herstellen und können  auch zum Färben von hochmolekularen plastischen  Massen oder für die Zubereitung von Farblacken ver  wendet werden.  



  Die Herstellung der neuen Farbstoffe erfordert  gegenüber den für diese     Farbstoffklasse        üblichen    Me  thoden keine neuen oder zusätzlichen Operationen.  Die Farbstoffe fügen sich vielmehr organisch der  Klasse der Eisfarben ein und stellen eine wesentliche       Bereicherung    und Erweiterung dieser     Farbstoffklasse     dar.    Die Herstellung der als     Diazokomponenten    ver  wendeten     o-Amino-azoverbindungen    kann nach be  kannten Methoden erfolgen.  



  <I>Beispiel</I>  36,4 g     2-Amino-4-methoxy-5-methyl-2'-methyl-          sulfonyl-4'-nitro-1,1'-azobenzol    in Form des     Diazo-          niumsulfates    werden in 4 Liter Wasser gelöst. Zu  dieser     Diazolösung    lässt man unter gutem Rühren eine  Lösung von 30 g     1-(2',3'-Oxy-naphthoylamino)-2-          methoxy-benzol    in verdünnter Natronlauge zulaufen.  Durch     allmähliches        Erwärmen    auf 90  C wird die  Kupplung beendet. Der gebildete     grünstichigschwarze     Farbstoff wird     abfiitriert,    gut ausgewaschen und ge  trocknet.  



  Man kann die Kupplung auch in Gegenwart eines  zur     Farblackherstellung    geeigneten Trägerstoffes vor  nehmen.  



  Die folgende Tabelle enthält noch eine Anzahl  von weiteren erfindungsgemäss verwendbaren Kom  ponenten sowie die Farbtöne der daraus erhältlichen       Azofarbstoffe,    die ebenfalls gute Echtheitseigenschaf  ten besitzen.    
EMI0002.0001     
  
    Diazokomponente <SEP> Azokomponente <SEP> Farbton
<tb>  2-Amino-4-methoxy-5-methyl-2'-methyl- <SEP> 1-(2',3'-Oxy-naphthoylamino)-4-chlor- <SEP> bräunliches
<tb>  sulfonyl-4'-nitro-1,1'-azobenzol <SEP> Benzol <SEP> Khaki
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-2-äthoxy- <SEP> grünes <SEP> Khaki
<tb>  Benzol
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-2,5- <SEP> grünstichiges
<tb>  dimethoxy-4-chlor-benzol <SEP> Khaki
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-4- <SEP> grünstichiges
<tb>  methoxy-benzol <SEP> Braun
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)

  -4-äthoxy- <SEP> grünstichiges
<tb>  Benzol <SEP> Braun
<tb>    <SEP> 2,3-Oxy-naphthoylamino-benzol <SEP> grünliches <SEP> Braun
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-3-nitro- <SEP> Khaki
<tb>  Benzol
<tb>  2-Amino-4-methoxy-5-äthyl-2'-methyl- <SEP> 2,3-Oxy-naphthoylamino-benzol <SEP> grünliches <SEP> Braun
<tb>  sulfonyl-4'-nitro-1,1'-azobenzol
<tb>  2-Amino-4-methoxy-5@methyl-2'-äthyl- <SEP> 1-(2',3'-Oxy-naphthoylamino)-2-methyl- <SEP> Graugrün
<tb>  sulfonyl-4'-nitro-1,1'-azobenzol <SEP> 4-methoxy-benzol
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-2- <SEP> Graugrün
<tb>  methyl-benzol
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-2,5- <SEP> gedecktes <SEP> bräun  dimethoxy-benzol <SEP> liches <SEP> Grün
<tb>  2-Amino-4-methoxy-5-methyl-2'-n- <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> bräunliches <SEP> Grün
<tb>  propylsulfonyl-4'-nitro-1,1'-azobenzol <SEP> 2,

  5-dimethoxy-benzol
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> bräunliches
<tb>  2-methoxy-4-chlor-5-methyl-benzol <SEP> Khaki
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> Graugrün
<tb>  2-methoxy-benzol
<tb>  2-Amino-4,5-dimethoxy-2'-methyl- <SEP> 1-(2',3'-Oxy-naphthoylamino)-2-methyl- <SEP> blaustichiges
<tb>  sulfonyl-4'-nitro-1, <SEP> l'-azobenzol <SEP> 4-methoxy-benzol <SEP> Graugrün
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> grünstichiges
<tb>  4-methoxy-benzol <SEP> Dunkelbraun
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-2-methyl- <SEP> grünliches
<tb>  Benzol <SEP> Blaugrau
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-naphthalin <SEP> grünliches <SEP> Khaki
<tb>    <SEP> 2-(2',3'-Oxy-naphthoylamino)-naphthalin <SEP> grünliches <SEP> Braun
<tb>  2-Amino-4,5-diäthoxy-2'-methylsulfonyl- <SEP> 1-(2',3'-Oxy-naphthoylamino)

  -naphthalin <SEP> gedecktes <SEP> Grün
<tb>  4'-nitro-1,1'-azobenzol
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> grünliches <SEP> Braun
<tb>  4-mothoxy-benzol
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> gedecktes <SEP> gelb  - <SEP> 2-methoxy-4-chlor-5-methyl-benzol <SEP> liches <SEP> Grün
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> Khaki
<tb>  2,4-d@imethoxy-5-chlor-benzol
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> grünliches <SEP> Braun
<tb>  2-methoxy-5-chlor-benzol       
EMI0003.0001     
  
    Diazokomponente <SEP> Azokomponente <SEP> Farbton
<tb>  2-Amino-4,5-diäthoxy-2'-methylsulfonyl- <SEP> 1-(2',3'-Oxy-naphthoylamino)-2-äthoxy- <SEP> gelbstickiges
<tb>  4'-nitro-1,1'-azobenzol <SEP> Benzol <SEP> Grün
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-4-äthoxy- <SEP> grünliches
<tb>  Benzol <SEP> Graubraun
<tb>    <SEP> 2-(2',

  3'-Oxy-naphthoylamino)- <SEP> grünliches <SEP> Oliv
<tb>  3-methoxy-diphenylenoxyd
<tb>    <SEP> 1-(6'-Brom-2',3'-oxy-naphthoylamino)- <SEP> grünliches <SEP> Oliv
<tb>  2-methoxy-benzol
<tb>  2-Amino-4,5-diäthoxy-2'-äthylsulfonyl- <SEP> 1-(2',3'-Oxy-naphthoylamino)-3-nitro- <SEP> gelbstickiges
<tb>  4'-nitro-1,1'-azobenzol <SEP> Benzol <SEP> Grün
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> gedecktes <SEP> Grün
<tb>  2,5-dimethoxy-benzol
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-2-methyl- <SEP> blaustichiges
<tb>  5-chlor-benzol <SEP> Grün
<tb>    <SEP> 1-(2',3'-Oxy-naph@thoylamino)-2-methyl- <SEP> gedecktes <SEP> Grün
<tb>  Benzol
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> bläuliches
<tb>  2,3-dimethyl-benzol <SEP> Graugrün
<tb>  2-Amino-4,5-diäthoxy-2'-n-propyl- <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> gelbstickiges
<tb>  sulfonyl-4'-nitro-1,

  1'-azobenzol <SEP> 2,4-dimethyl-benzol <SEP> Graugrün
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> gelbstickiges
<tb>  2-methoxy-5-chlor-benzol <SEP> Grün
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> stumpfes <SEP> Grün
<tb>  2-methoxy-4-chlor-5-methyl-benzol
<tb>  2-Amino-4,5-dimethoxy-2'-äthylsulfonyl- <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> gelbstickiges
<tb>  4'-nitro-1,1'-azobenzol <SEP> 2,5-dimethoxy-benzol <SEP> Grün
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-2-methyl- <SEP> Graugrün
<tb>  4-methoxy-benzol
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-2-äthoxy- <SEP> Graugrün
<tb>  Benzol
<tb>  2-Amino-4,5-dimethoxy-2'-n-propyl- <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> gelbstickiges
<tb>  sulfonyl-4'-nitro-1,1'-azobenzol <SEP> 2-methoxy-benzol <SEP> Grün
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> gelbstickiges
<tb>  2,

  5-dimethoxy-benzol <SEP> Grün
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-2-methyl- <SEP> gelbstickiges
<tb>  4-methoxy <SEP> Benzol <SEP> Grün
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> gelbstickiges
<tb>  2-methoxy-5-chlor-benzol <SEP> Graugrün
<tb>  2-Amino-4-methoxy-5-äthoxy-2'-methyl- <SEP> 2,3-Oxy-naphthoylamino <SEP> Benzol <SEP> Graugrün
<tb>  sulfonyl-4'-nitro-1,1'-azobenzol
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-2-methyl- <SEP> Graugrün
<tb>  4-chlor-benzol
<tb>  2-Amino-4,5-di-n-propoxy-2'-methyl- <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> stumpfes <SEP> Grün
<tb>  sulfonyl-4'-nitro-1,1'-azobenzol <SEP> 2-methoxy-4-chlor-5-methyl-benzol
<tb>    <SEP> 1-(2',3'-Oxy-naph#thoylamino)-2-methyl- <SEP> blaustichiges
<tb>  Benzol <SEP> Grün       
EMI0004.0001     
  
    Diazokomponente <SEP> Azokomponente <SEP> Farbton
<tb>  2 <SEP> Amino-4,

  5-di-n-propoxy-2'-methyl- <SEP> 1-(2',3'-Oxy-naphthoylamino)-2-äthoxy- <SEP> gedecktes <SEP> Grün
<tb>  sulfonyl-4'-nitro-1,1'-azobenzol <SEP> benzol
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-2-methyl- <SEP> blaustichiges
<tb>  4-methoxy-benzol <SEP> Grün
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> stumpfes <SEP> Grün
<tb>  2,4-dimethoxy-5-chlor-benzol
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> blaustichiges
<tb>  2,5-dimethoxy-benzol <SEP> Grün
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> stumpfes <SEP> Grün
<tb>  2-methoxy-5-chlor-benzol
<tb>  2-Amino-4-äthoxy-5-methoxy-2'-methyl- <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> gedecktes <SEP> Grün
<tb>  sulfonyl-4'-nitro-1,1'-azobenzol <SEP> 2-methoxy-benzol
<tb>    <SEP> 2,3-Oxy-naphthoylamino-benzol <SEP> Graugrün
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)

  -2-äthoxy- <SEP> gedecktes <SEP> Grün
<tb>  benzol
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)- <SEP> gelbstichiges
<tb>  2-methoxy-5-chlor-benzol <SEP> Graugrün
<tb>    <SEP> 1-(2',3'-Oxy-naphthoylamino)-4-methyl- <SEP> helles <SEP> Grauoliv
<tb>  benzol



  Process for the production of water-insoluble azo dyes It is known from German patent specification No. 609334 to produce water-insoluble dis.azo dyes by using diazotized substitution products of 2-amino-1,1'-azobenzene with oxyarylcarboxylic acid arylides,

          ss-ketocarboxylic acid esters and arylides or derivatives of pyrazolones by themselves. or clutches on a foundation. In this way, dyes are obtained which generally produce brown dyeings with good fastness properties on the fiber.



  It has now been found that valuable water-insoluble azo dyes are obtained if the diazonium compounds are derived from o-amino-azo compounds of the formula
EMI0001.0020
    wherein X denotes an alkyl or alkoxy group, couples with arylamides of 2,3-oxynaphthoic acid which contain no water-solubilizing groups.



  With the new dyes, greenish brown to green dyeings with good fastness properties are obtained on the vegetable fibers, including those made from regenerated cellulose, by the known dyeing processes, which have not yet been obtained in the ice dye series using suitable diazo components .



  The dyes can be produced in bulk or on a non-textile substrate and can also be used for dyeing high molecular weight plastic materials or for the preparation of colored lacquers.



  The preparation of the new dyes does not require any new or additional operations compared to the methods customary for this class of dyes. Rather, the dyes fit organically into the class of ice colors and represent an essential enrichment and expansion of this class of dyes. The o-amino-azo compounds used as diazo components can be prepared by known methods.



  <I> Example </I> 36.4 g of 2-amino-4-methoxy-5-methyl-2'-methyl-sulfonyl-4'-nitro-1,1'-azobenzene in the form of the diazonium sulfate are in 4 liters of water dissolved. A solution of 30 g of 1- (2 ', 3'-oxynaphthoylamino) -2-methoxy-benzene in dilute sodium hydroxide solution is allowed to run into this diazo solution with thorough stirring. The coupling is terminated by gradually heating to 90 ° C. The greenish black dye formed is filtered off, washed well and dried.



  The coupling can also be carried out in the presence of a carrier suitable for the production of colored varnishes.



  The following table also contains a number of further components which can be used according to the invention and the hues of the azo dyes obtainable therefrom, which likewise have good fastness properties.
EMI0002.0001
  
    Diazo component <SEP> azo component <SEP> color
<tb> 2-Amino-4-methoxy-5-methyl-2'-methyl- <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -4-chloro- <SEP> brownish
<tb> sulfonyl-4'-nitro-1,1'-azobenzene <SEP> benzene <SEP> khaki
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -2-ethoxy- <SEP> green <SEP> khaki
<tb> benzene
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -2,5- <SEP> greenish tint
<tb> dimethoxy-4-chloro-benzene <SEP> khaki
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -4- <SEP> greenish tint
<tb> methoxy-benzene <SEP> brown
<tb> <SEP> 1- (2 ', 3'-oxy-naphthoylamino)

  -4-ethoxy- <SEP> greenish tint
<tb> Benzene <SEP> brown
<tb> <SEP> 2,3-oxy-naphthoylamino-benzene <SEP> greenish <SEP> brown
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -3-nitro- <SEP> khaki
<tb> benzene
<tb> 2-Amino-4-methoxy-5-ethyl-2'-methyl- <SEP> 2,3-oxy-naphthoylamino-benzene <SEP> greenish <SEP> brown
<tb> sulfonyl-4'-nitro-1,1'-azobenzene
<tb> 2-Amino-4-methoxy-5 @ methyl-2'-ethyl- <SEP> 1- (2 ', 3'-oxy-naphthoylamino) -2-methyl- <SEP> gray-green
<tb> sulfonyl-4'-nitro-1,1'-azobenzene <SEP> 4-methoxy-benzene
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -2- <SEP> gray-green
<tb> methyl-benzene
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -2,5- <SEP> muted <SEP> brown dimethoxy-benzene <SEP> light <SEP> green
<tb> 2-Amino-4-methoxy-5-methyl-2'-n- <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> brownish <SEP> green
<tb> propylsulfonyl-4'-nitro-1,1'-azobenzene <SEP> 2,

  5-dimethoxy-benzene
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> brownish
<tb> 2-methoxy-4-chloro-5-methyl-benzene <SEP> khaki
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> gray-green
<tb> 2-methoxy-benzene
<tb> 2-Amino-4,5-dimethoxy-2'-methyl- <SEP> 1- (2 ', 3'-oxy-naphthoylamino) -2-methyl- <SEP> with a bluish tinge
<tb> sulfonyl-4'-nitro-1, <SEP> l'-azobenzene <SEP> 4-methoxy-benzene <SEP> gray-green
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> greenish
<tb> 4-methoxy-benzene <SEP> dark brown
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -2-methyl- <SEP> greenish
<tb> Benzene <SEP> blue-gray
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -naphthalene <SEP> greenish <SEP> khaki
<tb> <SEP> 2- (2 ', 3'-oxy-naphthoylamino) -naphthalene <SEP> greenish <SEP> brown
<tb> 2-Amino-4,5-diethoxy-2'-methylsulfonyl- <SEP> 1- (2 ', 3'-Oxy-naphthoylamino)

  -naphthalene <SEP> muted <SEP> green
<tb> 4'-nitro-1,1'-azobenzene
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> greenish <SEP> brown
<tb> 4-mothoxy-benzene
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> opaque <SEP> yellow - <SEP> 2-methoxy-4-chloro-5-methyl-benzene <SEP> liches < SEP> green
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> Khaki
<tb> 2,4-d @ imethoxy-5-chloro-benzene
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> greenish <SEP> brown
<tb> 2-methoxy-5-chlorobenzene
EMI0003.0001
  
    Diazo component <SEP> azo component <SEP> color
<tb> 2-Amino-4,5-diethoxy-2'-methylsulfonyl- <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -2-ethoxy- <SEP> yellow streaky
<tb> 4'-nitro-1,1'-azobenzene <SEP> benzene <SEP> green
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -4-ethoxy- <SEP> greenish
<tb> Benzene <SEP> gray-brown
<tb> <SEP> 2- (2 ',

  3'-oxy-naphthoylamino) - <SEP> greenish <SEP> olive
<tb> 3-methoxy-diphenylene oxide
<tb> <SEP> 1- (6'-bromo-2 ', 3'-oxy-naphthoylamino) - <SEP> greenish <SEP> olive
<tb> 2-methoxy-benzene
<tb> 2-Amino-4,5-diethoxy-2'-ethylsulfonyl- <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -3-nitro- <SEP> yellow streaky
<tb> 4'-nitro-1,1'-azobenzene <SEP> benzene <SEP> green
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> muted <SEP> green
<tb> 2,5-dimethoxy-benzene
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -2-methyl- <SEP> with a bluish tinge
<tb> 5-chloro-benzene <SEP> green
<tb> <SEP> 1- (2 ', 3'-Oxy-naph @ thoylamino) -2-methyl- <SEP> muted <SEP> green
<tb> benzene
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> bluish
<tb> 2,3-dimethyl-benzene <SEP> gray-green
<tb> 2-Amino-4,5-diethoxy-2'-n-propyl- <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> yellowish
<tb> sulfonyl-4'-nitro-1,

  1'-azobenzene <SEP> 2,4-dimethyl-benzene <SEP> gray-green
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> tinged yellow
<tb> 2-methoxy-5-chloro-benzene <SEP> green
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> dull <SEP> green
<tb> 2-methoxy-4-chloro-5-methyl-benzene
<tb> 2-Amino-4,5-dimethoxy-2'-ethylsulfonyl- <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> yellow-tinged
<tb> 4'-nitro-1,1'-azobenzene <SEP> 2,5-dimethoxy-benzene <SEP> green
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -2-methyl- <SEP> gray-green
<tb> 4-methoxy-benzene
<tb> <SEP> 1- (2 ', 3'-oxy-naphthoylamino) -2-ethoxy- <SEP> gray-green
<tb> benzene
<tb> 2-Amino-4,5-dimethoxy-2'-n-propyl- <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> yellow-tinged
<tb> sulfonyl-4'-nitro-1,1'-azobenzene <SEP> 2-methoxy-benzene <SEP> green
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> tinged yellow
<tb> 2,

  5-dimethoxy-benzene <SEP> green
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -2-methyl- <SEP> tinged yellow
<tb> 4-methoxy <SEP> Benzene <SEP> green
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> tinged yellow
<tb> 2-methoxy-5-chlorobenzene <SEP> gray-green
<tb> 2-Amino-4-methoxy-5-ethoxy-2'-methyl- <SEP> 2,3-oxy-naphthoylamino <SEP> Benzene <SEP> Gray-green
<tb> sulfonyl-4'-nitro-1,1'-azobenzene
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -2-methyl- <SEP> gray-green
<tb> 4-chlorobenzene
<tb> 2-Amino-4,5-di-n-propoxy-2'-methyl- <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> dull <SEP> green
<tb> sulfonyl-4'-nitro-1,1'-azobenzene <SEP> 2-methoxy-4-chloro-5-methyl-benzene
<tb> <SEP> 1- (2 ', 3'-Oxy-naph # thoylamino) -2-methyl- <SEP> with a bluish tinge
<tb> Benzene <SEP> Green
EMI0004.0001
  
    Diazo component <SEP> azo component <SEP> color
<tb> 2 <SEP> amino-4,

  5-di-n-propoxy-2'-methyl- <SEP> 1- (2 ', 3'-oxy-naphthoylamino) -2-ethoxy- <SEP> muted <SEP> green
<tb> sulfonyl-4'-nitro-1,1'-azobenzene <SEP> benzene
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -2-methyl- <SEP> with a bluish tinge
<tb> 4-methoxy-benzene <SEP> green
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> dull <SEP> green
<tb> 2,4-dimethoxy-5-chlorobenzene
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> bluish tint
<tb> 2,5-dimethoxy-benzene <SEP> green
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> dull <SEP> green
<tb> 2-methoxy-5-chlorobenzene
<tb> 2-Amino-4-ethoxy-5-methoxy-2'-methyl- <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> muted <SEP> green
<tb> sulfonyl-4'-nitro-1,1'-azobenzene <SEP> 2-methoxy-benzene
<tb> <SEP> 2,3-oxy-naphthoylamino-benzene <SEP> gray-green
<tb> <SEP> 1- (2 ', 3'-oxy-naphthoylamino)

  -2-ethoxy- <SEP> muted <SEP> green
<tb> benzene
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) - <SEP> yellowish
<tb> 2-methoxy-5-chlorobenzene <SEP> gray-green
<tb> <SEP> 1- (2 ', 3'-Oxy-naphthoylamino) -4-methyl- <SEP> light <SEP> gray olive
<tb> benzene

 

Claims (1)

PATENTANSPRUCH Verfahren zur Herstellung von wasserunlöslichen Azofarbstoffen, dadurch gekennzeichnet, dass man die Diazoniumverbindungen aus o-Amino-azoverbindun- gen der Formel EMI0004.0006 worin X eine Aikyl- oder Alkoxygruppe bedeutet, mit Arylamiden der 2,3-Oxy-naphthoesäure, die keine wasserlöslichmachenden Gruppen enthalten, kuppelt. PATENT CLAIM Process for the production of water-insoluble azo dyes, characterized in that the diazonium compounds from o-amino-azo compounds of the formula EMI0004.0006 wherein X is an alkyl or alkoxy group, couples with aryl amides of 2,3-oxynaphthoic acid which contain no water-solubilizing groups.
CH348762D 1956-06-27 1957-06-24 Process for the production of water-insoluble azo dyes CH348762A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE348762X 1956-06-27

Publications (1)

Publication Number Publication Date
CH348762A true CH348762A (en) 1960-09-15

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
CH348762D CH348762A (en) 1956-06-27 1957-06-24 Process for the production of water-insoluble azo dyes

Country Status (1)

Country Link
CH (1) CH348762A (en)

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