CH267310A - Process for the preparation of an azo dye. - Google Patents

Process for the preparation of an azo dye.

Info

Publication number
CH267310A
CH267310A CH267310DA CH267310A CH 267310 A CH267310 A CH 267310A CH 267310D A CH267310D A CH 267310DA CH 267310 A CH267310 A CH 267310A
Authority
CH
Switzerland
Prior art keywords
azo dye
preparation
dye
mol
amino
Prior art date
Application number
Other languages
German (de)
Inventor
Aktiengesellschaft Ciba
Original Assignee
Ciba Geigy
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 Ciba Geigy filed Critical Ciba Geigy
Publication of CH267310A publication Critical patent/CH267310A/en

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
    • C09B33/00Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
    • C09B33/02Disazo dyes
    • C09B33/12Disazo dyes in which the coupling component is a heterocyclic compound

Landscapes

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

Description

  

  Zusatzpatent zum Hauptpatent Nr. 261362.    Verfahren zur Herstellung eines     Azofarbstoffes.       Es wurde gefunden, dass ein wertvoller       Azofarbstoff    erhalten werden kann, wenn  man 2     Mol        diazotiertes    2-Amino-l-oxybenzol-  
EMI0001.0005     
    vereinigt.    Der neue Farbstoff stellt ein braunes  Pulver dar, das sich in Wasser und in kon  zentrierter Schwefelsäure mit gelber Farbe  löst und     Cellulosefasern    nach dem ein- oder       zweibadigen        Nachkupferungsverfahren    in     rot-          stiehig    gelben echten Tönen anfärbt.  



       2-Amino-l-oxybenzol-4-sulfonsäure        -,ss-        oxy-          äthylamid    kann nach an sich bekannter Me  thode hergestellt werden, indem man     2-Nitro-          1.-chlorbenzol-4-sulfonsäurechlorid    mit Mono  äthanolaniin umsetzt,

   durch Behandlung mit       Alkalihydroxyd    das Chloratom des     2-Nitro-l-          chlorbenzol    - 4 -     sulf        onsäure    -     fl    -     oxyäthylamids     durch die     Hydroxylgruppe    ersetzt und  schliesslich in der so erhaltenen     Nitroverbin-          dung    die     Nitrogruppe    zur     Aminogruppe    re  duziert.  



  Die Kupplungsreaktion kann beim vorlie  genden Verfahren in saurem, neutralem, vor  zugsweise aber alkalischem Medium. durch  geführt werden. Bei der Ausführung der  Kupplung in alkalischem Medium ist es vor  teilhaft, die Kupplungskomponente mit einem  geringen     f\berschuss    an     Alkalihydroxyd    zu         4-sulfonsäure-ss-oxyäthylamid    mit 1     Mol        1,1'-          [Diphenylen-    (4,4') ] -bis- (3     -methyl-    5 -     pyrazo-          lon)    der Formel    lösen, so dass sie in Form des     Dialkalisalzes     vorliegt und die weitere,

   für die Kupplung  benötigte     Alkalimenge    z. B. als     Alkalicarbo-          nat        hinzuzufügen.    Die Aufarbeitung des er  haltenen Farbstoffes kann in an sieh bekann  ter Weise erfolgen, z. B. durch     Abfiltrieren     und Trocknen.  



  <I>Beispiel:</I>  4,64 Teile     2-Amino-l-oxybenzol-4-sulfon-          säure-ss-oxyäthylamid    werden in üblicher  Weise in salzsaurer Lösung     diazotiert.    Die  erhaltene Suspension der     Diazoverbindung     wird durch Zugabe von Soda neutralisiert  und mit einer Lösung von 3,5 Teilen     1,1'-[Di-          phenylen-(4,4')        ]-bis-(3-methyl-5-pyrazolon)    in  40 Teilen 2,5     o/oiger    Natronlauge und 10 Teilen  10     o/oiger        Sodalösung    vereinigt.

   Nach been  deter     Kupplung    wird der abgeschiedene  Farbstoff     abfiltriert    und getrocknet.



  Additional patent to main patent no. 261362. Process for the production of an azo dye. It has been found that a valuable azo dye can be obtained if 2 moles of diazotized 2-amino-1-oxybenzene
EMI0001.0005
    united. The new dye is a brown powder that dissolves in water and in concentrated sulfuric acid with a yellow color and dyes cellulose fibers in real shades of reddish yellow using the one- or two-bath post-copper plating process.



       2-Amino-1-oxybenzene-4-sulfonic acid, ss- oxy- äthylamid can be prepared by a method known per se by reacting 2-nitro-1.-chlorobenzene-4-sulfonic acid chloride with monoethanolaniine,

   treatment with alkali hydroxide replaces the chlorine atom of 2-nitro-1-chlorobenzene-4-sulfonic acid-fl-oxyethyl amide with the hydroxyl group and finally reduces the nitro group to the amino group in the nitro compound thus obtained.



  In the present process, the coupling reaction can be carried out in an acidic, neutral, but preferably alkaline medium. be performed. When the coupling is carried out in an alkaline medium, it is advantageous to add 1 mol of 1,1'- [diphenylene- (4,4 ')] - to the coupling component with a slight excess of alkali metal hydroxide to form 4-sulfonic acid-ss-oxyethylamide Dissolve bis- (3 -methyl- 5-pyrazolone) of the formula so that it is present in the form of the dialkali salt and the further,

   amount of alkali required for the coupling z. B. to be added as alkali carbonate. The work-up of the dye he obtained can be done in a well-known manner, for. B. by filtering off and drying.



  <I> Example: </I> 4.64 parts of 2-amino-1-oxybenzene-4-sulfonic acid-ß-oxyethylamide are diazotized in a conventional manner in a hydrochloric acid solution. The suspension of the diazo compound obtained is neutralized by adding soda and treated with a solution of 3.5 parts of 1,1 '- [diphenylene- (4,4')] -bis- (3-methyl-5-pyrazolone) in 40 parts of 2.5% sodium hydroxide solution and 10 parts of 10% soda solution are combined.

   After coupling has been completed, the deposited dye is filtered off and dried.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines Azofarb- stoffes, dadurch gekennzeichnet, dass man 2 Mol diazotiertes 2-Amino-l-oxybeiizol-4-sul- fonsäure-ss-oxyäthylamid mit 1 Mol 1,1'-[Di- phenylen- (4,41)1 -bis-, (3-methyl-o"-pyrazolon) der Formel EMI0002.0005 vereinigt. PATENT CLAIM: Process for the production of an azo dye, characterized in that 2 mol of diazotized 2-amino-1-oxybeiizol-4-sulphonic acid-ss-oxyethylamide are mixed with 1 mol of 1,1 '- [diphenylene- (4 , 41) 1-bis-, (3-methyl-o "-pyrazolone) of the formula EMI0002.0005 united. Der neue Farbstoff stellt ein braunes Pulver dar, das sich in Wasser und in kon zentrierter Schwefelsäure mit gelber Farbe löst und Cellulosefasern nach dem ein- oder zweibadigen Nachleupferungsverfahren in rot- stiehig gelben echten Tönen anfärbt. The new dye is a brown powder that dissolves in water and in concentrated sulfuric acid with a yellow color and dyes cellulose fibers in reddish-yellow real shades using the one- or two-bath replenishment process.
CH267310D 1946-04-16 1946-04-16 Process for the preparation of an azo dye. CH267310A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH267310T 1946-04-16
CH261362T 1947-02-14

Publications (1)

Publication Number Publication Date
CH267310A true CH267310A (en) 1950-03-15

Family

ID=25730430

Family Applications (1)

Application Number Title Priority Date Filing Date
CH267310D CH267310A (en) 1946-04-16 1946-04-16 Process for the preparation of an azo dye.

Country Status (1)

Country Link
CH (1) CH267310A (en)

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