CH170933A - Process for the preparation of a 1-oxyalkylamino-4-arylaminoanthraquinone. - Google Patents

Process for the preparation of a 1-oxyalkylamino-4-arylaminoanthraquinone.

Info

Publication number
CH170933A
CH170933A CH170933DA CH170933A CH 170933 A CH170933 A CH 170933A CH 170933D A CH170933D A CH 170933DA CH 170933 A CH170933 A CH 170933A
Authority
CH
Switzerland
Prior art keywords
preparation
parts
oxyalkylamino
mol
arylaminoanthraquinone
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 CH170933A publication Critical patent/CH170933A/en

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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
    • C09B1/00Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16Amino-anthraquinones
    • C09B1/20Preparation from starting materials already containing the anthracene nucleus
    • C09B1/26Dyes with amino groups substituted by hydrocarbon radicals
    • C09B1/32Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
    • C09B1/325Dyes with no other substituents than the amino groups

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

      Zusatzpatent    zum     Hauptpatent    Nr. 166223.         Verfahren    zur Herstellung eines     1-Oxyalkylamino-4-arylitminoanthrachinons.       Es wurde gefunden, dass man ein     1-Oxyal-          kylarnirio-4-ai#ylamirioarithrachinon    erhalten  kann, wenn man auf 1     Mol        Leuko-1.4-di-(ss-          oxyäthylamino)-anthrachinon    1     Alol        1.4-Di-          aminobenzol    einwirken lässt und das so er  haltene Kondensationsprodukt oxydiert.  



  Die Oxydation kann durchgeführt werden,  indem das abgeschiedene Kondensationspro  dukt in einem besonderen Arbeitsgang oxy  diert wird; man kann auch das Oxydations  mittel während der Kondensation zugeben, es  findet dann Oxydation unmittelbar nach Kon  densation statt.  



  Das     1-ss-Oxyäthylamino-4-p-phenylendi-          aminoanthrachinon    bildet ein dunkles Pulver,  das sich in     llssigsäirreäthylester    mit grüner  Farbe löst. Nach geeigneter     Verpastung    färbt  es     Acetatkunstseide    in vollen und echten grünen  Tönen.  



  <I>Beispiel 1:</I>  6 Teile     Leuko-1.4-di(ss-oxyäthylamino)-          anthrachinon    werden in 30 Teilen Äthanol mit    2 Teilen     p-Phenylendiamin    und 1 Teil     p-Phe-          nylendiaminchlorhydrat    einige Stunden zum  Sieden erhitzt. Das gebildete Produkt wird  filtriert und in üblicher Weise oxydiert.    <I>Beispiel 2:</I>    8 Teile     Leuko-1.4-di(ss-oxyäthylamino)-          anthrachinon    werden in 35 Teilen     Methanol     mit 3 Teilen     1.4-Diaminobenzol,    0,7 Teilen       Natriumchlorat    und 2 Teilen Borsäure mehrere  Stunden auf 65   erhitzt.

   Man filtriert kalt,  wäscht mit Methanol und Wasser und erhält  in guter Ausbeute und Reinheit     1-p-Oxyäthyl-          amino-4-p-pheriylendiaminoanthrachirion.  



      Additional patent to main patent No. 166223. Process for the preparation of a 1-oxyalkylamino-4-arylitminoanthraquinone. It has been found that a 1-oxyalkylarnirio-4-ai # ylamirioarithraquinone can be obtained if 1 mol of leuco-1,4-di- (ss- oxyäthylamino) -anthraquinone 1 alol 1,4-diaminobenzene is allowed to act and that so he obtained condensation product is oxidized.



  The oxidation can be carried out by the deposited condensation product is oxidized in a special operation; you can also add the oxidizing agent during the condensation, then oxidation takes place immediately after the condensation.



  The 1-ss-oxyethylamino-4-p-phenylenediaminanthraquinone forms a dark powder which dissolves in ethyl acetate with a green color. After suitable pasting, it dyes acetate artificial silk in full and real green tones.



  <I> Example 1: </I> 6 parts of leuco-1,4-di (ss-oxyethylamino) anthraquinone are heated to boiling for a few hours in 30 parts of ethanol with 2 parts of p-phenylenediamine and 1 part of p-phenylenediamine chlorohydrate. The product formed is filtered and oxidized in the usual way. Example 2: 8 parts of leuco-1,4-di (ss-oxyethylamino) anthraquinone are heated to 65 for several hours in 35 parts of methanol with 3 parts of 1,4-diaminobenzene, 0.7 parts of sodium chlorate and 2 parts of boric acid .

   It is filtered cold, washed with methanol and water and 1-p-oxyethylamino-4-p-pheriylenediaminoanthrachirione is obtained in good yield and purity.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung von 1-p-Oxy- äthylamino-4-p-lphenylendiaminoarithrachinon, dadurch gekennzeichnet, dass man auf 1 Mol Leuko-l. 4-di-(ss-oxyäthylamino)-anthrachinon 1 Mol 1.4-Diaminobenzol einwirken lässt und das so erhaltene Kondensationsprodukt oxy diert. Das 1-ss-Ogyäthylamino-4-p-phenylendi- aminoanthrachinon bildet ein dunkles Pulver, das sich in Essigsäureäthylester mit grüner Farbe löst. PATENT CLAIM: Process for the preparation of 1-p-Oxy- äthylamino-4-p-1-phenylenediaminoarithraquinone, characterized in that 1 mol of leuco-l. 4-di- (ss-oxyäthylamino) anthraquinone allows 1 mol of 1,4-diaminobenzene to act and the condensation product thus obtained is oxidized. The 1-ss-Ogyäthylamino-4-p-phenylenedi-aminoanthraquinone forms a dark powder which dissolves in ethyl acetate with a green color. Nach geeigneter Verpastung färbt es Acetatkunstseide in vollen und echten grünen. Tönen. After suitable pasting, it dyes acetate artificial silk in full and real green. Tones.
CH170933D 1933-04-08 1933-04-08 Process for the preparation of a 1-oxyalkylamino-4-arylaminoanthraquinone. CH170933A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH170933T 1933-04-08
CH166223T 1934-02-06

Publications (1)

Publication Number Publication Date
CH170933A true CH170933A (en) 1934-07-31

Family

ID=25718257

Family Applications (1)

Application Number Title Priority Date Filing Date
CH170933D CH170933A (en) 1933-04-08 1933-04-08 Process for the preparation of a 1-oxyalkylamino-4-arylaminoanthraquinone.

Country Status (1)

Country Link
CH (1) CH170933A (en)

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