CH198321A - Process for the production of a new azo dye. - Google Patents

Process for the production of a new azo dye.

Info

Publication number
CH198321A
CH198321A CH198321DA CH198321A CH 198321 A CH198321 A CH 198321A CH 198321D A CH198321D A CH 198321DA CH 198321 A CH198321 A CH 198321A
Authority
CH
Switzerland
Prior art keywords
production
azo dye
new azo
new
dye
Prior art date
Application number
Other languages
German (de)
Inventor
Gesellschaft Fuer Chemis Basel
Original Assignee
Chem Ind Basel
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 Chem Ind Basel filed Critical Chem Ind Basel
Publication of CH198321A publication Critical patent/CH198321A/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00—Monoazo dyes prepared by diazotising and coupling
    • C09B29/32—Monoazo dyes prepared by diazotising and coupling from coupling components containing a reactive methylene group

Landscapes

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

Description

  

      Zusatzpatent,zum    Hauptpatent     Nr.   <B>195072.</B>    Verfahren zur 'Herstellung eines neuen     Azofarbstoffes.       Es wurde     gefünclen"dass    man einen neuen       Azofarbstoff        #erhä,1t,    wenn     man        diazotiertes          1-Aminoi2#-nitrobenzo,1    mit dem     Arylid,    das  erhalten wird     durcli    Kondensieren von  <B>5</B>     -Amino-        methoxy)        -phenyl-ps,eudo,

  -azi-          m--idobenzol        mü,        Acetessigester,    vereinigt.  



  Der neue Farbstoff bildet ein gelbes, in  Wasser unlösliches, Pulver. Auf geeigneten       ,Subsüaten,    wie z. B. Baumwolle, hergestellt,       fKrbt    er diese in echten. gelben Tönen.  



  <I>Beispiel:</I>  <B><I>13 A</I></B>     Tdle        o-Nitranil-in    werden, wie üblich.       ,cliazotiert    und in eine Lösung -von 32,4 Tei  len des Kondensationsproduktes aus 5-Amino       2-(4'--methox-y)-phen,yl-pseudo-azi,miclo,benzol-          mit        Acetessigester,   <B>10.0</B> Teilen     Natrium-          hy#c1Toxyd-lösung    von<B>3,6 '</B> B6,<B>15</B> Teilen         Na,triumacetat    und 20010 Teilen Wasser ein  getragen. Der     gebilclete    gelbe Farbstoff fällt  sofort aus. Er wird filtriert und getrocknet.



      Additional patent, to the main patent no. <B> 195072. </B> Process for the 'production of a new azo dye. It was found that a new azo dye was obtained when diazotized 1-amino-nitrobenzo-1 with the arylide obtained by condensing 5-amino-methoxy-phenyl -pseudo,

  -azim - idobenzol mü, acetoacetic ester, combined.



  The new dye forms a yellow powder that is insoluble in water. On suitable sub-seeds such B. Cotton, if he dyes them in real. yellow tones.



  <I> Example: </I> <B> <I> 13 A </I> </B> Tdle o-nitranil-in will be as usual. , cliazotized and in a solution of 32.4 parts of the condensation product of 5-amino 2- (4 '- methox-y) -phen, yl-pseudo-azi, miclo, benzene- with acetoacetic ester, <B> 10.0 </B> parts sodium hy # c1 oxide solution of <B> 3.6 '</B> B6, <B> 15 </B> parts sodium trium acetate and 20,010 parts water. The colored yellow dye precipitates immediately. It is filtered and dried.

Claims (1)

<B>PATENTANSPRUCH:</B> Verfahren zur Ilerstellung eines neuen Azofarbstoffes, dadurch gekennzeichnet, dass man diazotiertes 1-Amino-2-nitro-benzo,1 mit ,dem Aryl-id, das erhalten wird duxe,11 Künden- sieren von 5-Anuno-2#-(4'-methoxy)-phenyl- ps,eu-do-azi-mi,dobenzol mitAcetessigester, ver einigt. Der neue Farbstoff bildet ein gelbes, in Wasser unlösliches Pulver. Auf geeigneten iSubstraten, wie z. Claim: Process for the production of a new azo dye, characterized in that diazotized 1-amino-2-nitro-benzo, 1 with, the aryl-id that is obtained, is duxed 11 Künd- sieren of 5-Anuno-2 # - (4'-methoxy) -phenyl-ps, eu-do-azi-mi, dobenzene with acetoacetic ester, combined. The new dye forms a yellow powder that is insoluble in water. On suitable iSubstrates, such as. R Baumwolle, hergestellt, fäx,bt er diese in. echten gelben Tönen. R cotton, manufactured, fax, he practices this in real yellow tones.
CH198321D 1936-07-14 1936-07-14 Process for the production of a new azo dye. CH198321A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH195072T 1936-07-14
CH198321T 1936-07-14

Publications (1)

Publication Number Publication Date
CH198321A true CH198321A (en) 1938-06-15

Family

ID=25722723

Family Applications (1)

Application Number Title Priority Date Filing Date
CH198321D CH198321A (en) 1936-07-14 1936-07-14 Process for the production of a new azo dye.

Country Status (1)

Country Link
CH (1) CH198321A (en)

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