DE530292C - Process for the preparation of 2-aroylbenzanthrones - Google Patents

Process for the preparation of 2-aroylbenzanthrones

Info

Publication number
DE530292C
DE530292C DEI39655D DEI0039655D DE530292C DE 530292 C DE530292 C DE 530292C DE I39655 D DEI39655 D DE I39655D DE I0039655 D DEI0039655 D DE I0039655D DE 530292 C DE530292 C DE 530292C
Authority
DE
Germany
Prior art keywords
parts
preparation
aroylbenzanthrones
product
solution
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
DEI39655D
Other languages
German (de)
Inventor
Dr Willy Eichholz
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to DEI39655D priority Critical patent/DE530292C/en
Application granted granted Critical
Publication of DE530292C publication Critical patent/DE530292C/en
Expired legal-status Critical Current

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
    • C09B3/02Benzathrones
    • C09B3/06Preparation from starting materials already containing the benzanthrone nucleus

Description

Verfahren zur Darstellung von 2-Aroylbenzanthronen Es wurde gefunden, daß man 2-Aroylben.zanthrone erhält, wenn man die nach dein ,erfahren des Patents 501 082 durch alkalische Kondensation von Benzanthrön oder seinen Substitutionsprodukten mit N itrilen der Formel R - C I-12 - C N erhältlichen Produkte der allgemeinen Formel in Gegenwart organischer Verdiinnungsmittel mit Oxydationsmitteln behandelt.Process for the preparation of 2-aroylbenzanthrones It has been found that 2-aroylbenzanthrones are obtained if, according to your experience of patent 501 082, by alkaline condensation of benzanthron or its substitution products with nitriles of the formula R - C I-12 - CN available products of the general formula treated with oxidizing agents in the presence of organic thinners.

Beispiel i io Teile des Kondensationsproduktes aus Benzanthron und Benzylcyanid (erhältlich nach Beispiel :2 des Patents 5oi o82) werden in 20o Teilen Eisessig mit io Teilen Natriumbichromat so lange zum Sieden erhitzt, bis in einer Probe kein Ausgangsmaterial mehr nachzuweisen ist. Nimmt man die Oxydation bei niedrigerer Temperatur vor, so verläuft sie entsprechend langsamer. Das nach dem Erkalten der Lösung mit Wasser ausgefällte Rohprodukt kann zu weiterer Reinigung im Hochvakuum sublimiert oder aus einem geeigneten Lösungsmittel, z. B. Eisessig, umkristallisiert - werden. Das so in gelben Nadeln erhaltene Produkt stellt nach Analyse und Reaktionen 2-Benzoylbenzanthron dar. Es ist in organischen Lösungsmitteln in der Kälte schwer, in der Hitze verhältnismäßig leicht löslich. Seine Lösungsfarbe in konzentrierter Schwefelsäure ist Rot. Beispiel :2 io Teile des Kondensationsproduktes aus m-Benzanthron und p-Chlorbenzylcyanid (dargestellt in analoger Weise wie das in Beispiel i verwendete Ausgangsmaterial) werden in einer Lösung von io Teilen Natriumhichromat in 2oö Teilen Eisessig etwa i Stunde lang zum Sieden erhitzt. Das beim Erkalten in gelben Nadeln auskristallisierende Produkt stellt praktisch reines 2-p-Chlorbenzoylbenzanthron dar. Seine Eigenschaften sind denen des unsubstituierten Produktes sehr ähnlich.Example i io parts of the condensation product from benzanthrone and Benzyl cyanide (obtainable according to example: 2 of the patent 5oi o82) are in 20o parts Glacial acetic acid with 10 parts of sodium dichromate heated to boiling until in one Sample no more starting material can be detected. If you take the oxidation at lower Temperature, it is correspondingly slower. After the Solution with water precipitated crude product can be used for further purification in a high vacuum sublimed or from a suitable solvent, e.g. B. glacial acetic acid, recrystallized - will. The product obtained in this way in yellow needles presents itself after analysis and reactions 2-Benzoylbenzanthron. It is difficult in organic solvents in the cold to Relatively easily soluble in the heat. His solution color in more concentrated Sulfuric acid is red. Example: 2 10 parts of the condensation product from m-benzanthrone and p-chlorobenzyl cyanide (prepared in a manner analogous to that used in Example i Starting material) are dissolved in a solution of 10 parts of sodium dichromate in 2oö parts Heated glacial acetic acid to the boil for about an hour. When it cools in yellow needles The product which crystallizes out is practically pure 2-p-chlorobenzoylbenzanthrone Its properties are very similar to those of the unsubstituted product.

Beispiel g Die Lösung bzw. Suspension von io Teilen des in Beispiel i verwendeten Ausgangsmaterials in ioo Teilen Aceton wird unter Rühren langsam, so daß die Temperatur 300 nicht übersteigt, mit. -einerLösurig bzw. Suspension von 5 Teilen Kaliumpermanganat in ioo Teilen Aeeton.versetz"t. Nach Beendigung der Oxydation wird mit verdünnter Schwefelsäure angesäuert und durch Zugabe von Natriumbisulfitlösung der Braunstein entfernt. Das nach dem Absaugen erhaltene Produkt kann nach den in Beispiel z beschriebenen Methoden gereinigt werden und ist mit dem dort erhaltenen Produkt identisch.Example g The solution or suspension of 10 parts of the in example i used starting material in ioo parts acetone is taking stir slowly so that the temperature does not exceed 300 with. -a solution or suspension of 5 parts of potassium permanganate in 100 parts of aeeton Oxidation is acidified with dilute sulfuric acid and by adding sodium bisulfite solution the brownstone removed. The product obtained after suction can be processed according to the in Example z described methods are cleaned and is with the one obtained there Identical product.

Claims (1)

PATENTANSPRUCH: Verfahren zur Darstellung von 2-Aroylben,zanthronen, dadurch gekennzeichnet, daß man die nach .dem Verfahren des Patents 5oI o82 durch alkalische Kondensation von Benzanthron oder seinen Substitutionsproidukten mit Nitrilen der Formel R - C H2 - C: N erhältlichen Produkte der allgemeinen Formel in Gegenwart organischer Verdünnungsmittel mit Oxydationsmitteln behandelt.PATENT CLAIM: Process for the preparation of 2-aroylbenes, zanthrones, characterized in that the general products obtainable according to the process of the patent 5oI o82 by alkaline condensation of benzanthrone or its substitution products with nitriles of the formula R - C H2 - C: N formula treated with oxidizing agents in the presence of organic diluents.
DEI39655D 1929-10-26 1929-10-26 Process for the preparation of 2-aroylbenzanthrones Expired DE530292C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEI39655D DE530292C (en) 1929-10-26 1929-10-26 Process for the preparation of 2-aroylbenzanthrones

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEI39655D DE530292C (en) 1929-10-26 1929-10-26 Process for the preparation of 2-aroylbenzanthrones

Publications (1)

Publication Number Publication Date
DE530292C true DE530292C (en) 1931-07-25

Family

ID=7190110

Family Applications (1)

Application Number Title Priority Date Filing Date
DEI39655D Expired DE530292C (en) 1929-10-26 1929-10-26 Process for the preparation of 2-aroylbenzanthrones

Country Status (1)

Country Link
DE (1) DE530292C (en)

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