CH130616A - Process for the production of a new dye. - Google Patents

Process for the production of a new dye.

Info

Publication number
CH130616A
CH130616A CH130616DA CH130616A CH 130616 A CH130616 A CH 130616A CH 130616D A CH130616D A CH 130616DA CH 130616 A CH130616 A CH 130616A
Authority
CH
Switzerland
Prior art keywords
blue
dissolves
vat
violet
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 CH130616A publication Critical patent/CH130616A/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
    • C09B3/00Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
    • C09B3/22Dibenzanthrones; Isodibenzanthrones
    • C09B3/30Preparation from starting materials already containing the dibenzanthrone or isodibenzanthrone nucleus
    • C09B3/32Preparation from starting materials already containing the dibenzanthrone or isodibenzanthrone nucleus by halogenation

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

Description

  

      Zusatzpatent    zum Hauptpatent Nr. 119986.    verfahren zur Herstellung eines neuen     Farbstoffes.       Im Hauptpatent Nr. 119986 ist ein neues  Halogenderivat des     Dibenzanthrons        besehrie-          ben,    das sich von den bereits bekannten Ha  logenderivaten des     Dibenzanthrons    durch  den blauen Farbton und durch die Wasser  echtheit seiner Baumwollfärbungen aus  zeichnet.  



  Es wurde nun gefunden, dass es auch       gelingt,    durch Behandeln des     Dibenzanthrons          finit    so viel     Ferrichlorid,    dass' das erhaltene  chlorhaltige Produkt die Baumwolle aus der       Küpe    in blauen, wasserechten Tönen färbt,  einen dem Produkt des Hauptpatentes voll  ständig ebenbürtigen Farbstoff zu erhalten.  



  Der Farbstoff löst sich in konzentrierter  Schwefelsäure     violettblau;    diese Lösung, in  Wasser gegossen. fällt blaue Flocken. In  siedendem Nitrobenzol und     Trichlorbenzol     löst er sich     violettblau    mit intensiv braun  roter Fluoreszenz, in siedendem Anilin       violettstichig    blau. Die     Küpe    ist     grünstichig     blau.    <I>Beispiel:</I>  10 Teile reines     Dibenzanthron    werden  in 250 Teilen     Trichlorbenzol    suspendiert,  die Suspension unter Rühren auf 140' er  wärmt und darauf langsam 60 Teile wasser  freies Eisenchlorid eingetragen.

   Man hält  während     erogen    Stunden die Temperatur bei  140 bis<B>150'.</B> Die     Chlorierung    geht unter  starker     Salzsäuregasentwicklung    vor sich.  Die Reaktionsmasse wird dann mit Wasser  dampf behandelt, der isolierte Farbstoff mit       verdünnter    Salzsäure extrahiert, filtriert und  getrocknet. In guter Ausbeute erhält man  ein dunkelblaues     Farbstoffpulver,    welches  die Baumwolle aus der     Küpe    in blauen, nicht  wasserempfindlichen Tönen färbt..



      Additional patent to main patent no. 119986. Process for the production of a new dye. The main patent No. 119986 describes a new halogen derivative of dibenzanthrone, which is distinguished from the already known halogen derivatives of dibenzanthrone by its blue color and the waterfastness of its cotton dyes.



  It has now been found that by treating the dibenzanthrone finite enough ferric chloride that the chlorine-containing product obtained dyes the cotton from the vat in blue, water-fast tones, it is possible to obtain a dye that is completely equal to the product of the main patent.



  The dye dissolves in concentrated sulfuric acid violet blue; this solution, poured into water. falls blue flakes. In boiling nitrobenzene and trichlorobenzene it dissolves violet-blue with intense brown-red fluorescence, in boiling aniline it dissolves violet-tinged blue. The vat is blue with a green tinge. <I> Example: </I> 10 parts of pure dibenzanthrone are suspended in 250 parts of trichlorobenzene, the suspension is heated to 140 ° with stirring and then 60 parts of anhydrous iron chloride are slowly added.

   The temperature is maintained at 140 to 150 'for erogenous hours. The chlorination proceeds with vigorous evolution of hydrochloric acid gas. The reaction mass is then treated with steam, the isolated dye extracted with dilute hydrochloric acid, filtered and dried. A dark blue dye powder is obtained in good yield, which dyes the cotton from the vat in blue, water-insensitive shades.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines Küpen- farbstoffes der Dibenzanthronreihe, dadurch gekennzeichnet, dass Dibenzanthron mit so viel Ferrichlorid behandelt wird, dass das erhaltene chlorhaltige Produkt die Baum- wolle aus der Küpe in blauen, wasserechten Tönen färbt. - --- - Der Farbstoff löst sich in konzentrierter Schwefelsäure violettblau; diese Lösung, in Wasser gegossen. fällt blaue Flocken. PATENT CLAIM: Process for the production of a vat dye of the dibenzanthrone series, characterized in that dibenzanthrone is treated with so much ferric chloride that the chlorine-containing product obtained dyes the cotton from the vat in blue, water-fast tones. - --- - The dye dissolves in concentrated sulfuric acid violet blue; this solution, poured into water. falls blue flakes. In siedendem Nitrobenzol und Trichlorbenzoi löst er sich violettblau mit intensiv braun roter Fluoreszenz, in siedendem Anilin violettstichig blau. Die Küpe ist grünstichig blau. In boiling nitrobenzene and trichlorobenzene it dissolves violet-blue with intense brown-red fluorescence, in boiling aniline it dissolves violet-tinged blue. The vat is blue with a green tinge.
CH130616D 1927-07-21 1927-07-21 Process for the production of a new dye. CH130616A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH130616T 1927-07-21
CH119986T 1928-07-04

Publications (1)

Publication Number Publication Date
CH130616A true CH130616A (en) 1928-12-15

Family

ID=25709376

Family Applications (1)

Application Number Title Priority Date Filing Date
CH130616D CH130616A (en) 1927-07-21 1927-07-21 Process for the production of a new dye.

Country Status (1)

Country Link
CH (1) CH130616A (en)

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