CH234515A - Process for the production of a urea derivative. - Google Patents

Process for the production of a urea derivative.

Info

Publication number
CH234515A
CH234515A CH234515DA CH234515A CH 234515 A CH234515 A CH 234515A CH 234515D A CH234515D A CH 234515DA CH 234515 A CH234515 A CH 234515A
Authority
CH
Switzerland
Prior art keywords
production
urea derivative
weight
parts
sodium
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 CH234515A publication Critical patent/CH234515A/en

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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
    • C09B43/00—Preparation of azo dyes from other azo compounds
    • C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups
    • C09B43/136—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents
    • C09B43/14—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents with phosgene or thiophosgene

Landscapes

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

Description

  

  <B>Zusatzpatent</B> zum     Hauptpatent    Nr. 232121.    Verfahren zur Herstellung eines     Rarnstoifderivates.            Es,        wurde        ,gefunden,        @dass        mam.    zu einem       neuen        Harnstoffderivat    gelangt,

   das     gleich-          zeitig        einen        wertvollen        Azo        arbs        toff        darstellt.          wenn    man auf 2     Mäl    :der     2-M.ethyl-4-(4"-          amnn@o)-        bonzayl:amina    - 2' -     oxy,-1,1'-azob@enzol-          3'-ca.rbansäure-5'-sulfonsäuTe    1     Mol        Phosgen          einwirken    lässt.  



  Der neue     Farbistoff        stellt        ein'    braunes       Pulver    dar, :das. Baumwolle in     :sehwach        alka-          lischem    Bade, das     mit        einer        Kupfersalzlösung     aus     Kupfersulfat    und     Weinsaurem        Natrium          versetzt    wurde, in     waschechtem        rotstichig          gelbem    Tone anfärbt.

      <I>Beispiel:</I>       70,2     des     Mon@oazo@farb:stoffes     aus     :diazotierter        1-Amino-2-oxybenz,ol-3-carb-          ogy-5-sulfonsäure        und        1-Methyl-3raminoben-          zol    werden     als        Na-Salz    unter Zusatz von 27       GewicMsteilen        Natriumacetat    in 500     Ge-          wiehtsbeilen    Wasser :

  gelöst.     Diese    Lösung  wird bei     etwa>    60  mit 3,9     Gewichtsteilen        4-          Nitrobenzoyl.chlori,d,    die mit 10     Gewichts-          teilen    Aceton     versetzt        wurden,    behandelt.

    Man     reduziert        Idas        ,gebildete        Nitroben@zo.yl-          pro@dukt    mit 84     Gewichtsteilen        kristaläsier-          +em        Natriumsulfid,    die in 150 Gewichtstei-         len        Wasser    gelöst     wurden,    bei 65=70  zum       Aminob,enzoylpr        odukt.    Das.

       abgeschiedene     Reduktionsprodukt wird     unter    Zusatz von       Nabriumcarbonat    bis zur     deutlichen    alka  lischen Reaktion in. 4000     Gewichtsteilen     Wasser gelöst und während     24,Stunden    unter  Rühren bei ss0'-40  mit     Phosgen    behandelt,  bis sich keine freie     NHZ!Grupp:

  e    mehr     naeh-          w@eis@en        lässt.    Das     aus,gescMedene        Harn@stof'f-          derivat        wird    a     ls        Natriums@alz    gefällt,     filtriemt     und     .getrocknet.  



  <B> Additional patent </B> to main patent No. 232121. Process for the production of a raw material derivative. It was found @that mam. arrives at a new urea derivative,

   which at the same time is a valuable azo substance. if one on 2 times: der 2-M.ethyl-4- (4 "- amnn @ o) - bonzayl: amina - 2 '- oxy, -1,1'-azob @ enzol- 3'-ca.rbansäure- 5'-sulfonic acid allows 1 mol of phosgene to act.



  The new dye is a 'brown powder: that. Cotton in a very awake alkaline bath to which a copper salt solution of copper sulfate and tartaric acid sodium has been added, dyes in a washable, reddish yellow shade.

      <I> Example: </I> 70.2 of the Mon @ oazo @ color: substance made from: diazotized 1-amino-2-oxybenz, ol-3-carbogy-5-sulfonic acid and 1-methyl-3raminobenzene are used as sodium salt with the addition of 27 parts by weight of sodium acetate in 500 parts by weight of water:

  solved. This solution is treated at about> 60 with 3.9 parts by weight of 4-nitrobenzoyl.chlori, d to which 10 parts by weight of acetone have been added.

    Idas, formed nitrobenzzo.yl product is reduced with 84 parts by weight of crystallized sodium sulfide, which were dissolved in 150 parts by weight of water, at 65 = 70 to the aminobenezoyl product. The.

       The deposited reduction product is dissolved in 4000 parts by weight of water with the addition of nabrium carbonate until a clear alkaline reaction is obtained and treated with phosgene for 24 hours with stirring at ss0'-40 until no free NHZ!

  e more naeh- w @ eis @ en lets. The urea derivative, which has been mixed out, is precipitated as sodium salt, filtered and dried.

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines lIam- lerivates, dadurch gekennzeichnet, d@ass <I>s</I> toffc man auf 2 Mol der 2-Methyl-4a(4"-amino) benizoylamino,-2'--ogy-1,1'-azobenzol-3'-carbon- s,äure-5',sulfons#äure 1 Mel Phosgen einwir ken lässt. Der neue Pambisto, PATENT CLAIM: A process for the production of a lam- lerivates, characterized in that d @ ass <I> s </I> toffc one to 2 moles of the 2-methyl-4a (4 "-amino) benizoylamino, -2 '- ogy- 1,1'-azobenzene-3'-carbon- s, acid-5 ', sulfonic acid 1 Mel phosgene can act. The new Pambisto, ff stellt ein braunes Pulver dar, das Baumwolle in sohwacb, alka- lischem Bade, das mit einer aus Kupfersulfat und weinsaurem Natrium versetzt wunde, in waschechtem rotstichig gelbem Tone anfärbt. ff represents a brown powder that stains cotton in sohwacb, alkaline bath that has a wound made of copper sulfate and tartrate of sodium in a washable, reddish-yellow shade.
CH234515D 1940-11-22 1940-11-22 Process for the production of a urea derivative. CH234515A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH232121T 1940-11-22
CH234515T 1940-11-22

Publications (1)

Publication Number Publication Date
CH234515A true CH234515A (en) 1944-09-30

Family

ID=25727673

Family Applications (1)

Application Number Title Priority Date Filing Date
CH234515D CH234515A (en) 1940-11-22 1940-11-22 Process for the production of a urea derivative.

Country Status (1)

Country Link
CH (1) CH234515A (en)

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