CH220650A - Process for the production of a new azo dye. - Google Patents

Process for the production of a new azo dye.

Info

Publication number
CH220650A
CH220650A CH220650DA CH220650A CH 220650 A CH220650 A CH 220650A CH 220650D A CH220650D A CH 220650DA CH 220650 A CH220650 A CH 220650A
Authority
CH
Switzerland
Prior art keywords
mole
amino
production
new
product
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 CH220650A publication Critical patent/CH220650A/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
    • C09B43/136Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents
    • C09B43/16Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents linking amino-azo or cyanuric acid residues

Description

  

  <B>Zusatzpatent</B> zum     Hauptpatent    Nr. 217241.    Verfahren zur Herstellung eines neuen     AzofarbstofFes.       Es wurde gefunden,     dass    man einen  neuen     Azofarbstoff    erhält, wenn man 1     Mol          Cyanurchlorid,    1     Mol    der     1-Amino-4-(4'-          amino-        3'-sulf        o)-anilidoanthrachinon-2-sulf        on-          säure,    1     Mol    des     Produktes,

      das erhalten  wird     durch        Reduzieren    .des     A.cylierungs-          produktes    aus 1     Mol        meta-Nitrobenzoylchlo-          rid    und 1     Mol        4-Amino-4'-ogy-1,1'-azobenzol-          3'-carbonsäure    und 1     Mol        Anilin    aufeinander  einwirken lässt.

   Der neue Farbstoff stellt ein       dunkles    Pulver .dar, das sich in Wasser mit  grüner Farbe löst und Baumwolle in schwach  alkalischem Bade in Gegenwart von Kupfer  sulfat und weinsaurem Natrium in     wasch-          und    lichtechten grünen Tönen färbt.

      <I>Beispiel:</I>  48,'9 Gewichtsteile     1-Amino-4-(4'-amino-          3'    -     sulfo)    -     anilidoanthraehinon    -'2     -sulfonsäure     werden als neutrale Lösung in 1000     Ge-          wichtsteilen    Wasser zu einer     Anschlämmung     von 18.5 Gewichtsteilen     Cyanurchlorid    in  500 Gewichtsteilen kaltem     Wasser        gegeben.       Man hält die Temperatur 4     ,Stunden    bei 10  bis 15  .

   Die bei der     Kondensation    ent  stehende     Salzsäure        wird    durch die entspre  chende Menge     Natriumcarbonat        neutralisiert.     Hernach werden 37;

  6     Gewichtsteile        Jes    Pro  duktes, das erhalten wird durch Reduzieren  des     Acylierungsproduktes        aus        meta-Nitro-          benzoylchlorid    und     4-Amino-4'-ogy-1,1'-azo-          benzol-,3'-carbonsäure    in 50,0 Gewichtsteilen  warmem     Wasser    gelöst, zum     Monokondeiuea-          tionsprodukt    .gegeben. Die Temperatur     wird     dabei auf 40   erhöht.

   Nach 24     Stunden    .gibt       man    18 Gewichtsteile     Anilin    zu und hält die  Temperatur während der     ,gleichen    Zeit auf  80  . Das     tertiäre        Kondensationsprodukt        ist     nach dieser Zeit     .gebildet,    Es wird mit     Na-          triumehlorid        abgeschieden    und getrocknet.



  <B> Additional patent </B> to main patent no. 217241. Process for the production of a new azo dye. It has been found that a new azo dye is obtained when 1 mole of cyanuric chloride, 1 mole of 1-amino-4- (4'-amino-3'-sulfo) -anilidoanthraquinone-2-sulfonic acid, 1 mole of the product,

      this is obtained by reducing the acylation product from 1 mole of meta-nitrobenzoyl chloride and 1 mole of 4-amino-4'-ogy-1,1'-azobenzene-3'-carboxylic acid and 1 mole of aniline .

   The new dye is a dark powder that dissolves in water with a green color and colors cotton in a weakly alkaline bath in the presence of copper sulfate and tartrate of sodium in washable and lightfast green tones.

      <I> Example: </I> 48, '9 parts by weight of 1-amino-4- (4'-amino-3' - sulfo) - anilidoanthraehinone -'2 -sulfonic acid become a neutral solution in 1000 parts by weight of water Added suspension of 18.5 parts by weight of cyanuric chloride in 500 parts by weight of cold water. The temperature is maintained at 10 to 15 hours for 4 hours.

   The hydrochloric acid formed during the condensation is neutralized by the appropriate amount of sodium carbonate. Afterwards 37;

  6 parts by weight of Jes Pro products, which is obtained by reducing the acylation product from meta-nitrobenzoyl chloride and 4-amino-4'-ogy-1,1'-azo-benzene, 3'-carboxylic acid in 50.0 parts by weight of warm water dissolved, given to the monoconduction product. The temperature is increased to 40.

   After 24 hours, 18 parts by weight of aniline are added and the temperature is maintained at 80 for the same time. The tertiary condensation product is formed after this time. It is deposited with sodium chloride and dried.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines neuen Azofaxbstoffe@s, dadurch gekennzeichnet, dass man 1 Mol Cyanurchlorid, 1 Mol der 1-Amino-4-(4'-amino-3'-sulfo)-anilidoanthra- chinon-2-sulfonsäure, 1 Mol des Produktes, PATENT CLAIM: A process for the production of a new Azofaxbstoffe @ s, characterized in that 1 mol of cyanuric chloride, 1 mol of 1-amino-4- (4'-amino-3'-sulfo) -anilidoanthraquinone-2-sulfonic acid, 1 Moles of product, das erhalten wird durch Reduzieren des Aev- lierungsproduktes aus 1 Mol meta-Nitro- benzoylchlorid und 1 Mol d- Amino-4'-oxy- 1,1'-azobenzol-3'-carbonsäure und 1 Mol Ani lin aufeinander einwirken lässt. this is obtained by reducing the evaporation product from 1 mole of meta-nitrobenzoyl chloride and 1 mole of d-amino-4'-oxy-1,1'-azobenzene-3'-carboxylic acid and 1 mole of aniline. Der neue Farbstoff stellt ein dunkles Pulver dar, Glas sich in Wasser mit grüner Farbe löst und Baumwolle in schwach alkalischem Bade in Gegenwart von Kupfersulfat und wein saurem Natrium in wasch- und lichtechten grünen Tönen. färbt. The new dye is a dark powder, glass dissolves in water with a green color and cotton in a weakly alkaline bath in the presence of copper sulphate and acidic sodium in washable and lightfast green tones. colors.
CH220650D 1940-07-09 1940-07-09 Process for the production of a new azo dye. CH220650A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH220650T 1940-07-09
CH217241T 1940-07-09

Publications (1)

Publication Number Publication Date
CH220650A true CH220650A (en) 1942-04-15

Family

ID=25725993

Family Applications (1)

Application Number Title Priority Date Filing Date
CH220650D CH220650A (en) 1940-07-09 1940-07-09 Process for the production of a new azo dye.

Country Status (1)

Country Link
CH (1) CH220650A (en)

Similar Documents

Publication Publication Date Title
CH220650A (en) Process for the production of a new azo dye.
CH220648A (en) Process for the production of a new azo dye.
CH217241A (en) Process for the production of a new azo dye.
CH220653A (en) Process for the production of a new azo dye.
CH220647A (en) Process for the production of a new azo dye.
CH220646A (en) Process for the production of a new azo dye.
CH220651A (en) Process for the production of a new azo dye.
CH220649A (en) Process for the production of a new azo dye.
CH220652A (en) Process for the production of a new azo dye.
CH220645A (en) Process for the production of a new azo dye.
CH217958A (en) Process for the preparation of a polyazo dye.
AT133505B (en) Process for the preparation of ω-Oxyacylaminobenzolarsin- or -stibinoxden or ω-Oxyacylaminobenzolarsin- or -stibinsäuren.
CH217959A (en) Process for the preparation of a polyazo dye.
CH217965A (en) Process for the preparation of a polyazo dye.
CH215147A (en) Process for the preparation of a polyazo dye.
CH131254A (en) Process for the production of a new azo dye.
CH131503A (en) Process for the production of a new chromium-containing azo dye.
CH217960A (en) Process for the preparation of a polyazo dye.
CH302049A (en) Process for the preparation of a disazo dye.
CH217492A (en) Process for the preparation of an azo dye.
CH232296A (en) Process for the production of a new azo dye.
CH220431A (en) Process for the preparation of an azo dye.
CH166087A (en) Process for the production of a new metal-containing dye.
CH183114A (en) Process for the preparation of an azo dye.
CH148967A (en) Process for the preparation of a diazoamino compound.