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CH233348A - Process for the preparation of a tetrakisazo dye. - Google Patents

Process for the preparation of a tetrakisazo dye.

Info

Publication number
CH233348A
CH233348A CH233348DA CH233348A CH 233348 A CH233348 A CH 233348A CH 233348D A CH233348D A CH 233348DA CH 233348 A CH233348 A CH 233348A
Authority
CH
Switzerland
Prior art keywords
dye
weight
parts
amino
preparation
Prior art date
Application number
Other languages
German (de)
Inventor
Aktiengesellsc Farbenindustrie
Original Assignee
Ig Farbenindustrie 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 Ig Farbenindustrie Ag filed Critical Ig Farbenindustrie Ag
Publication of CH233348A publication Critical patent/CH233348A/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
    • C09B33/18Trisazo or higher polyazo dyes
    • C09B33/28Tetrazo dyes of the type A->B->K<-C<-D

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

Description

  

      Zusatzpatent    zum Hauptpatent Nr. 229425.    Verfahren zur Herstellung eines     Tetrakisazofarbstoffes.       Vorliegende Erfindung betrifft ein Ver  fahren zur     Herstellung    eines     T@trakisazofarb-          otoffes.    Das Verfahren     besteht        :darin,    -dass  man     diazotierte        5-(4'-Aminobenzoylamino)-2-          oxybenzol    -1-     carbonsäure    mit     1-Amino    -     2-          m:

  ethylbenzol    vereinigt, den erhaltenen       Aminoazofarbstoff        weiterdiazotiert    und mit  dem symmetrischen     Harnstoff    aus     2-Amino-          5-oxynaphthalin-7-sulfonsäure    kuppelt.  



  Der neue     Farbstoff    stellt ein :dunkles       wasiserlösliches    Pulver :dar, :das vegetabilische  Fasern in     blaustichig    roten Tönen färbt.  



       Beispiel:     272 Gewichtsteile     5-(4'-Aminobenzoyl-          5        amino)-2-oxybenzol-l-carbonsäure    werden in  4000     Gewichtsteilen    Wasser     unter    Zusatz von  140 Gewichtsteilen     Natriumcarbonat        _    warm       g        g        elöst.        Nach        Zugabe        von        69        Gewichtsteilen          Natriumnitrit    wird abgekühlt und die Lösung  o in 500 

  Gewichtsteile Salzsäure (d = 1,18)  und 3500 Gewichtsteile Eis langsam einge  rührt. Die gelbe     Diazoniumverbindung    fällt    aus und wird nach 11/2 Stunden mit einer  Lösung von 107     Gewichtsteilen        1-Amino-2-          methylbenzol    in 85     Gewichtsteilen    Salzsäure  (d =1.,18),     verdünnt    mit     wenig    Wasser, ver  setzt.

   Man stumpft mit etwa 700 Gewichts=  teilen einer 30 %     igen        wässrigen        Natrium-          acetatlösung    .ganz langsam ab und isoliert  den     Aminoazofarbstoff    in üblicher Weise.  



  Zur weiteren     Diazotierung    wird das Zwi  schenprodukt mit 4000 Gewichtsteilen Was  iser erneut     angeschlämmt.    Es werden 69 Ge  wichtsteile     Natriumnitrit    und 500 Gewichts  teile Salzsäure     (d    = 1,18) nacheinander zu  gefügt.

   Man     diazotiert    2 Stunden bei     Zim-          mertemperatur    und trägt :die erhaltene dicke  Paste in     eine    Lösung des     Natriumsalzes    von  252 Gewichtsteilen des symmetrischen Harn  stoffes     aus    2     -Amino    - 5 -     oxynaphthalin    -7-     sul-          fonsäure    ein. Die Kupplung wird durch  langsame Zugabe einer Lösung von 70 Ge  wichtsteilen     Natriumcarbonat    in Wasser be  schleunigt und ist nach 2     ,Stunden    beendet.

    Der     Farbstoff        wird    heiss mit     wenig,Salz    aus-      gesalzen, filtriert     und    getrocknet. Der so     her-          gestellte        Tetrakvsazofarbstoff    stellt ein,dunk  les wasserlösliches Pulver dar, das vegetabi  lische Fasern in blaustichig     roten    Tönen an  färbt. Die     Nassechtheit    der Färbungen wird  durch Nachbehandlung mit Chromsalzen ver  bessert, ohne dass sich der Farbton     wesentlich     ändert.



      Additional patent to main patent No. 229425. Process for the production of a tetrakisazo dye. The present invention relates to a method for producing a T @ trakisazofarb- otoffes. The process consists of: -that diazotized 5- (4'-aminobenzoylamino) -2- oxybenzene -1-carboxylic acid with 1-amino - 2- m:

  ethylbenzene combined, the aminoazo dye obtained further diazotized and coupled with the symmetrical urea from 2-amino-5-oxynaphthalene-7-sulfonic acid.



  The new dye is a: dark washer-soluble powder: is,: that dyes vegetable fibers in bluish red tones.



       Example: 272 parts by weight of 5- (4'-aminobenzoyl-5 amino) -2-oxybenzene-1-carboxylic acid are dissolved in 4000 parts by weight of water with the addition of 140 parts by weight of hot sodium carbonate. After adding 69 parts by weight of sodium nitrite, the mixture is cooled and the solution o in 500

  Parts by weight of hydrochloric acid (d = 1.18) and 3500 parts by weight of ice are slowly stirred in. The yellow diazonium compound precipitates and is after 11/2 hours with a solution of 107 parts by weight of 1-amino-2-methylbenzene in 85 parts by weight of hydrochloric acid (d = 1., 18), diluted with a little water, ver sets.

   About 700 parts by weight of a 30% strength aqueous sodium acetate solution are blunted very slowly and the aminoazo dye is isolated in the usual way.



  For further diazotization, the inter mediate product is slurried again with 4000 parts by weight of water. 69 parts by weight of sodium nitrite and 500 parts by weight of hydrochloric acid (d = 1.18) are added one after the other.

   The mixture is diazotized for 2 hours at room temperature and the thick paste obtained is added to a solution of the sodium salt of 252 parts by weight of the symmetrical urea from 2-amino-5-oxynaphthalene-7-sulphonic acid. The coupling is accelerated by the slow addition of a solution of 70 parts by weight of sodium carbonate in water and is complete after 2 hours.

    The dye is salted out hot with a little salt, filtered and dried. The tetrakosazo dye produced in this way is a dark, water-soluble powder that stains vegetable fibers in bluish red tones. The wet fastness of the dyeings is improved by aftertreatment with chromium salts without the color shade changing significantly.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines Tet.ra- kisazofarbstoffes, dadurch gekennzeichnet, .dass man dianotierte 5-j(4'-Aminobenzoyl- am@ino)-?-oxj-benzol-l-ca.rbonsäure mit. 1- Amino-2-mcthylbenzol vereinigt, den erhalte nen Aminoazofarbstoff weiterdiazotiert und mit dem symmetrischen Harnstoff aus 2- Amino-5-oxynaphthalin-7-sulfonsäure kup pelt. PATENT CLAIM: Process for the production of a tetrakisazo dye, characterized in that dianotated 5-j (4'-aminobenzoyl- am @ ino) -? - oxj-benzene-l-carboxylic acid is used with. 1- Amino-2-methylbenzene combined, the aminoazo dye obtained is further diazotized and kup pelt with the symmetrical urea from 2- amino-5-oxynaphthalene-7-sulfonic acid. Der neue Farbsloff stellt eindunkles was serlösliches Pulver dar, das vegetabilische Fasern in roten Tönen färbt. The new dye is a dark, water-soluble powder that dyes vegetable fibers in red tones.
CH233348D 1941-06-09 1942-05-28 Process for the preparation of a tetrakisazo dye. CH233348A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE233348X 1941-06-09
CH229425T 1942-05-28

Publications (1)

Publication Number Publication Date
CH233348A true CH233348A (en) 1944-07-15

Family

ID=25727352

Family Applications (1)

Application Number Title Priority Date Filing Date
CH233348D CH233348A (en) 1941-06-09 1942-05-28 Process for the preparation of a tetrakisazo dye.

Country Status (1)

Country Link
CH (1) CH233348A (en)

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