CH188779A - Process for the preparation of an insoluble azo dye. - Google Patents

Process for the preparation of an insoluble azo dye.

Info

Publication number
CH188779A
CH188779A CH188779DA CH188779A CH 188779 A CH188779 A CH 188779A CH 188779D A CH188779D A CH 188779DA CH 188779 A CH188779 A CH 188779A
Authority
CH
Switzerland
Prior art keywords
azo dye
insoluble azo
preparation
dye
aminobenzene
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 CH188779A publication Critical patent/CH188779A/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
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/34Monoazo dyes prepared by diazotising and coupling from other coupling components
    • C09B29/36Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
    • C09B29/3604Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
    • C09B29/3617Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom
    • C09B29/3643Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from quinolines or hydrogenated quinolines

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

Description

  

      Zusatzpatent    zum Hauptpatent Nr. 185944.         Verfahren    zur Herstellung eines unlöslichen     Azofarbstoffes.       Gemäss dem im Hauptpatent beschriebe  nen Verfahren erhält man einen     Acetatseide     in blaustichig roten Tönen anfärbenden un  löslichen     Azofarbstoff,    wenn man     4-Nitro-l-          aminobenzol        diazotiert    und die     Diazoverbin-          dung    mit     1-Butyl-3-oxy-7-chlortetrahydrochi-          nolin    kuppelt.  



  Wie nun weiter gefunden wurde, erhält  man einen     Farbstoff    von ähnlichen Eigen  schaften, wenn man     6-Chlor-2.        4-dinitro-l-          aminobenzol        diazotiert    und die     Diazoverbin-          dung    mit     1-n-Butyl-3-methoxy-7-methyl-          tetrahydrochinolin    kuppelt.

      <I>Beispiel:</I>    21,8 Teile     6-Chlor-2.4-dinitro-l-amino-          benzol    werden in der üblichen Weise     diazo-          tiert.    Die     Diazoverbindung    lässt man in eine  eisgekühlte Lösung von 24,6     Teilen.    1-n-         Butyl-3-methoxy-    7     -methyl-tetrahydrochino-          lin    in der entsprechenden     Menge    verdünnter  Salzsäure einlaufen und stumpft zur Been  digung der Kupplung mit     Natriumacetat    ab.

    Der erhaltene Farbstoff färbt     Acetatseide    im       Seifensuspensionsbad    rötlich blau.



      Additional patent to main patent no. 185944. Process for the production of an insoluble azo dye. According to the process described in the main patent, an insoluble azo dye which stains acetate silk in bluish red shades is obtained if 4-nitro-l-aminobenzene is diazotized and the diazo compound is coupled with 1-butyl-3-oxy-7-chlorotetrahydroquinoline .



  As has now been found further, a dye of similar properties is obtained if 6-chloro-2. 4-dinitro-l-aminobenzene is diazotized and the diazo compound is coupled with 1-n-butyl-3-methoxy-7-methyl-tetrahydroquinoline.

      <I> Example: </I> 21.8 parts of 6-chloro-2,4-dinitro-1-aminobenzene are diazo- tated in the usual way. The diazo compound is left in an ice-cold solution of 24.6 parts. 1-n-Butyl-3-methoxy-7-methyl-tetrahydroquinoline is poured in in the appropriate amount of dilute hydrochloric acid and blunted with sodium acetate to complete the coupling.

    The dye obtained gives the acetate silk a reddish blue color in the soap suspension bath.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines unlös lichen Azofarbstoffes, dadurch gekennzeich net, dass man 6-Chlor-2.4-dinitro-l-amino- benzol diazotiert und die Diazoverbindung mit 1-n-Butyl-3-methogy- 7 -methyl-tetra- hydrochinolin kuppelt. Der erhaltene Farbstoff färbt Acetatseide rötlich blau:. PATENT CLAIM: Process for the production of an insoluble azo dye, characterized in that 6-chloro-2,4-dinitro-l-aminobenzene is diazotized and the diazo compound is treated with 1-n-butyl-3-methogy- 7 -methyl-tetra- hydroquinoline couples. The dye obtained dyes acetate silk reddish blue :.
CH188779D 1935-05-07 1936-03-26 Process for the preparation of an insoluble azo dye. CH188779A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH185944T 1935-05-07
CH188779T 1936-03-26

Publications (1)

Publication Number Publication Date
CH188779A true CH188779A (en) 1937-01-15

Family

ID=25721273

Family Applications (1)

Application Number Title Priority Date Filing Date
CH188779D CH188779A (en) 1935-05-07 1936-03-26 Process for the preparation of an insoluble azo dye.

Country Status (1)

Country Link
CH (1) CH188779A (en)

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