CH110416A - Process for the preparation of an anthracene derivative. - Google Patents

Process for the preparation of an anthracene derivative.

Info

Publication number
CH110416A
CH110416A CH110416DA CH110416A CH 110416 A CH110416 A CH 110416A CH 110416D A CH110416D A CH 110416DA CH 110416 A CH110416 A CH 110416A
Authority
CH
Switzerland
Prior art keywords
anthracene derivative
yellow
anthraquinone
brown
preparation
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 CH110416A publication Critical patent/CH110416A/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
    • C09B5/00Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
    • C09B5/24Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being only condensed with an anthraquinone nucleus in 1-2 or 2-3 position

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

Description

  

  verfahren zur .Herstellung eines     Anthraeenderivates.       Es wurde gefunden; dass man ein neues       Anthracenderivat    enthält, wenn man ein     An-          thrachinon-2-glyzin-3-karbonsäure    mit Kon  densationsmitteln behandelt.  



  Das neue     Anthracenderivat,    das als ein  Abkömmling des     2,3-Anthrachinonindoxyls     aufzufassen ist, bildet     bräunlichgelbe    Kristalle,  welche sich in kalter, konzentrierter Schwefel  säure mit orangeroter Farbe lösen und mit  Wasser als     grünlichgelbe    Flocken ausgefällt  werden. In Nitrobenzol ist es mit gelbbrauner  Farbe löslich. Mit     Hydrosulfit    und Natron  lauge entsteht eine     Küpe,    die zunächst braun  ist und nach einiger Zeit nach     olivegrün    um  schlägt. Es bildet ein wertvolles Ausgangs  material zur Darstellung von Farbstoffen.

         Beispiel:     29 Teile     Arithrachinon-2-glyzin-3-karbon-          säure    und 15. Teile entwässertes Natrium  acetat werden in 290 Teilen     Essigsäurean-          hydrid    einige Zeit rückfliessend gekocht. Vor  übergehend entsteht eine .braune Lösung,    woraus sich nach kurzer Zeit     bräunlichgelbe     Kristalle' abscheiden. Diese werden nach dem  Erkalten abgesaugt, zuerst mit Eisessig, dann  mit Wasser gewaschen und getrocknet.



  process for .production of an anthraeene derivative. It was found; that one contains a new anthracene derivative if one treats an anthrachinone-2-glycine-3-carboxylic acid with condensation agents.



  The new anthracene derivative, which is to be understood as a derivative of 2,3-anthraquinone indoxyl, forms brownish-yellow crystals, which dissolve in cold, concentrated sulfuric acid with an orange-red color and are precipitated as greenish-yellow flakes with water. It is soluble in nitrobenzene with a yellow-brown color. With hydrosulphite and caustic soda, a vat is created that is initially brown and then turns olive-green after a while. It is a valuable starting material for the representation of dyes.

         Example: 29 parts of arithraquinone-2-glycine-3-carbonic acid and 15 parts of dehydrated sodium acetate are refluxed for some time in 290 parts of acetic anhydride. A "brown solution" is formed before a transition, from which brownish-yellow crystals separate out after a short time. After cooling, these are suctioned off, washed first with glacial acetic acid, then with water and dried.

 

Claims (1)

P9TENTANSPRUCH: Verfahren zur Herstellung eines Anthra- cenderivates, dadurch gekennzeichnet, dass man die Anthrachinon-2-glyzin-3-karbonsäure mit Kondensationsmitteln behandelt. Das neue Anthracenderivat, das als ein Abkömmling des 2,3-Anthrachinonindoxyls . aufzufassen ist, bildet bräunliehgelbe Kristalle, welche sich. in kalter, konzentrierter Schwefel säure mit orangeroter Farbe lösen und mit Wasser als grünlichgelbe Flocken ausgefällt werden. In Nitrobenzol ist es mit gelbbrauner Farbe löslich. P9TENT CLAIM: Process for the production of an anthracene derivative, characterized in that the anthraquinone-2-glycine-3-carboxylic acid is treated with condensing agents. The new anthracene derivative that is derived from 2,3-anthraquinone indoxyl. is to be understood, forms brownish yellow crystals, which are. Dissolve in cold, concentrated sulfuric acid with an orange-red color and precipitate with water as greenish-yellow flakes. It is soluble in nitrobenzene with a yellow-brown color. Mit Hydrosulfit und Natron lauge entsteht eine Küpe, die zunächst braun ist und nach einiger Zeit nach olivegrün umschlägt. Es bildet ein wertvolles Ausgangs material zur Darstellung von Farbstoffen. With hydrosulphite and caustic soda, a vat is created that is initially brown and then turns olive-green after a while. It is a valuable starting material for the representation of dyes.
CH110416D 1923-01-24 1923-11-30 Process for the preparation of an anthracene derivative. CH110416A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH103648T 1923-01-24
CH110416T 1923-11-30

Publications (1)

Publication Number Publication Date
CH110416A true CH110416A (en) 1925-06-01

Family

ID=25706525

Family Applications (1)

Application Number Title Priority Date Filing Date
CH110416D CH110416A (en) 1923-01-24 1923-11-30 Process for the preparation of an anthracene derivative.

Country Status (1)

Country Link
CH (1) CH110416A (en)

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