CH209533A - Process for the preparation of a new derivative of an azo dye. - Google Patents

Process for the preparation of a new derivative of an azo dye.

Info

Publication number
CH209533A
CH209533A CH209533DA CH209533A CH 209533 A CH209533 A CH 209533A CH 209533D A CH209533D A CH 209533DA CH 209533 A CH209533 A CH 209533A
Authority
CH
Switzerland
Prior art keywords
dye
preparation
azo dye
new derivative
mol
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 CH209533A publication Critical patent/CH209533A/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
    • C09B43/00Preparation of azo dyes from other azo compounds
    • C09B43/12Preparation of azo dyes from other azo compounds by acylation of amino groups

Landscapes

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

Description

  

  Zusatzpatent zum Hauptpatent     Nr.    205164.    Verfahren zur Herstellung eines neuen Derivates eines     Azofarbstoffes.       Es wurde gefunden,     dass    man ein neues  Derivat eines     Azofarbstoffes    erhält, wenn man  <B>1</B>     Mol    des     Trisazofarbstoffes,    der erhalten  wird durch Vereinigen eines Moleküls der       1,3-Diaminobenzol-4-sulfonsäure    mit<B>1</B>     Mol     des     diazotierten        Disazofarbstoffes    aus     diazo-          tierter        2-Amiiioiiaphtbalin-4,

  8-disulfonsäure     und<B>1</B>     Amino-S-methylberizol,        Weiterdiazo-          tieren    und Vereinigen mit einem zweiten  Molekül     1-Amiiio-S-methylbeiizol,    mit 2     Mol          Benzoylohlorid    in Gegenwart einer tertiären  Base     acyliert.     



  Der neue Farbstoff stellt ein braunes  Pulver dar und färbt Baumwolle in echten  braunorangen Tönen.  



  <I>Beispiel:</I>  <B>1</B>     Mol    des     Trisazofarbstoffes,    der erhalten  wird durch Vereinigen der     1,3-Diaminobenzol-          4-stilfotisäure    mit dem     diazotierten        Di8azo-          farbstoff    aus     diazotierter        2-Aminoinaphthalin-          4,8-disulfonsäure    und     1-Arnino-3-methylbenzol,          Weiterdiazotieren    und Vereinigen mit<B>1</B>     Mol          1-Amino-B-methylbenzol,

      wird in der<B>10-</B> bis  15fachen Menge des     Pyridins    gelöst und bei    400 mit 2     Mol        Benzoylchlorid    versetzt. Man  erwärmt allmählich auf<B>900</B> und hält diese  Temperatur eine Stunde. Nach dieser Zeit  wird das     Dibenzoylprodukt    abgeschieden und       getrockn    et.



  Additional patent to main patent no. 205164. Process for the production of a new derivative of an azo dye. It has been found that a new derivative of an azo dye is obtained if <B> 1 </B> moles of the trisazo dye obtained by combining a molecule of 1,3-diaminobenzene-4-sulfonic acid with <B> 1 < / B> mol of the diazotized disazo dye from diazo- tated 2-Amiiioiiaphtbalin-4,

  8-disulfonic acid and <B> 1 </B> amino-S-methylberizole, further diazo- ting and combining with a second molecule of 1-amino-S-methylbeiizole, acylated with 2 moles of benzoylochloride in the presence of a tertiary base.



  The new dye is a brown powder and dyes cotton in real brown-orange tones.



  <I> Example: </I> <B> 1 </B> mol of the trisazo dye, which is obtained by combining the 1,3-diaminobenzene-4-stilphotic acid with the diazotized di8azo dye from diazotized 2-aminoinaphthalene-4, 8-disulfonic acid and 1-amino-3-methylbenzene, further diazotizing and combining with <B> 1 </B> mol of 1-amino-B-methylbenzene,

      is dissolved in <B> 10 </B> to 15 times the amount of pyridine and mixed with 2 mol of benzoyl chloride at 400. The temperature is gradually increased to <B> 900 </B> and held for one hour. After this time, the dibenzoyl product is deposited and getrockn et.

 

Claims (1)

PATENTANSPRUCII: Verfahren zur Herstellung eines neuen Derivates eines Azofarbstoffes, dadurch ge kennzeichnet, dass man<B>1</B> Mol des Trisazo- farbstoffes, der erhalten wird durch Vereinigen eines Moleküls der 1,3-Diaminobenzol-4-sul- fonsäure mit<B>1</B> Mol des diazotierten Disazo- farbstoffes aus diazotierter 2-Aminonaph- thalin-4, PATENT CLAIM: Process for the preparation of a new derivative of an azo dye, characterized in that <B> 1 </B> mol of the trisazo dye which is obtained by combining a molecule of 1,3-diaminobenzene-4-sulphonic acid with <B> 1 </B> mol of the diazotized disazo dye from diazotized 2-aminonaphthalene-4, 8-disulfonsäure und 1-Ai-üino-3-me- thylbenzol, Weiterdiazotieren und Vereinigen mit einem zweiten Molekül 1-Amino-3-methyl- benzol, mit 2 Mol Benzoylchlorid in Gegen wart einer tertiären Base acyliert. Der neue Farbstoff stellt ein braunes Pulver dar und färbt Baumwolle in echten braunorangen Tönen. 8-disulfonic acid and 1-aluino-3-methylbenzene, further diazotizing and combining with a second molecule of 1-amino-3-methylbenzene, acylated with 2 moles of benzoyl chloride in the presence of a tertiary base. The new dye is a brown powder and dyes cotton in real brown-orange tones.
CH209533D 1937-01-26 1937-01-26 Process for the preparation of a new derivative of an azo dye. CH209533A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH209533T 1937-01-26
CH205164T 1939-02-01

Publications (1)

Publication Number Publication Date
CH209533A true CH209533A (en) 1940-04-15

Family

ID=25724120

Family Applications (1)

Application Number Title Priority Date Filing Date
CH209533D CH209533A (en) 1937-01-26 1937-01-26 Process for the preparation of a new derivative of an azo dye.

Country Status (1)

Country Link
CH (1) CH209533A (en)

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