DE492275C - Process for the preparation of Kuepen dyes - Google Patents

Process for the preparation of Kuepen dyes

Info

Publication number
DE492275C
DE492275C DEI29597D DEI0029597D DE492275C DE 492275 C DE492275 C DE 492275C DE I29597 D DEI29597 D DE I29597D DE I0029597 D DEI0029597 D DE I0029597D DE 492275 C DE492275 C DE 492275C
Authority
DE
Germany
Prior art keywords
preparation
dyes
weight
parts
dye
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
DEI29597D
Other languages
German (de)
Inventor
Dr Karl Wilke
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 DEI29597D priority Critical patent/DE492275C/en
Application granted granted Critical
Publication of DE492275C publication Critical patent/DE492275C/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
    • C09B5/00Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
    • C09B5/02Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position
    • C09B5/04Pyrazolanthrones
    • C09B5/06Benzanthronyl-pyrazolanthrone condensation products

Description

Verfahren zur Darstellung von Küpenfarbstoffen Es wurde gefunden, daß durch Einwirkung nitrierender Mittel auf Benzanthronpyrazolanthron mit oder ohne nachfolgende Reduktion neue Farbstoffe entstehen, die färberisch ähnlich wertvolle Eigenschaften aufweisen, wie die nitrierten Farbstoffe der Dibenzanthronreihe (vgl. die deutsche Patentschrift 185 222). Beispiel i In eine Suspension von io Gewichtsteilen Benzanthronpyrazolanthron (vgl. die Patentschrift 490723, Beispiel i) in 5o Gewichtsteilen Eisessig läßt man ein. Gemisch von 2o Gewichtsteilen Salpetersäure von 48' B6 und 3o Gewichtsteilen Eisessig einlaufen und verrührt bei gewöhnlicher Temperatur etwa 15 Stunden lang. Dann wird filtriert und mit Eisessig gewaschen. Man erhält eine schwarzviolette Farbstoffpaste, getrocknet ein violettschwarzes Pulver, das sich in Schwefelsäure von 96 °Jo mit grüner Farbe löst. Beim Verdünnen wird diese Lösung zunächst gelbstichiger grün und läßt dann violette Flocken fallen. Aus blauer alkalischer Hydrosulfitküpe färbt der Farbstoff auf Baumwolle ein schönes klares Grün, das beim Chloren nach Grau bis Schwarz umschlägt.Process for the preparation of vat dyes It was found that by the action of nitrating agents on Benzanthronpyrazolanthron with or without subsequent reduction, new dyes are created that are of similar value in terms of color Have properties like the nitrated dyes of the dibenzanthrone series (cf. German patent specification 185 222). Example i In a suspension of 10 parts by weight Benzanthronpyrazolanthron (cf. Patent 490723, Example i) in 50 parts by weight One lets in glacial acetic acid. Mixture of 20 parts by weight of nitric acid from 48 'B6 and Pour in 3o parts by weight of glacial acetic acid and stir at normal temperature for about For 15 hours. It is then filtered and washed with glacial acetic acid. You get one black-purple dye paste, a purple-black powder that is dried Dissolves in sulfuric acid of 96 ° Jo with a green color. When diluted, this solution becomes first yellowish green and then drops violet flakes. From blue alkaline Hydrosulphite vat turns the dye on cotton a beautiful clear green, which when Chlorine turns gray to black.

Ein ähnliches Produkt erhält man bei kurzer Einwirkung von konzentrierter Salpetersäure auf Benzanthronpyrazolanthron in Nitrobenzol.A similar product is obtained with a short exposure to concentrated Nitric acid on benzanthrone pyrazole anthrone in nitrobenzene.

Beispiel 2 Das Produkt der Kalischmelze von Benzanthronylpyrazolanthron bei höherer Temperatur (vgl. Patentschrift 490723, Beispiel 2) liefert bei der Nitrierung nach Beispiel i einen Farbstoff, der aus grüner Lösung in konzentrierter Schwefelsäure beim Verdünnen in grünschwarzen Flocken ausfällt und Baumwolle aus blauer Küpe in olivegrauen Tönen anfärbt. Beim Chloren werden diese Färbungen wenig heller. Beispiel 3 =o Gewichtsteile des nach Beispiel i gewonnenen Farbstoffes werden aus Schwefelsäure umgefällt und in dünner Paste nach Zugabe von 6o bis 7o Gewichtsteilen kristallisierten Schwefelnatriums mehrere Stunden lang auf dem Dampfbade erwärmt. Dann wird filtriert und gewaschen, die erhaltene dunkelgrüne Farbstoffpaste gegebenenfalls getrocknet. Das Produkt verhält sich färberisch wie der urreduzierte Farbstoff. Konzentrierte Schwefelsäure löst es zum Unterschiede von jenem mit roter Farbe.Example 2 The product of the potash melt of benzanthronylpyrazolanthrone at a higher temperature (cf. patent specification 490723, example 2) yields a dye in the nitration according to example i, which precipitates from green solution in concentrated sulfuric acid when diluted in greenish-black flakes and cotton from a blue vat in olive-gray Colors tones. With chlorination, these colors become a little lighter. Example 3 = 0 parts by weight of the dye obtained according to Example 1 are reprecipitated from sulfuric acid and, after the addition of 60 to 70 parts by weight of crystallized sodium sulphide, heated in a thin paste for several hours on the steam bath. It is then filtered and washed, and the dark green dye paste obtained is optionally dried. In terms of color, the product behaves like the reduced dye. Concentrated sulfuric acid dissolves it to distinguish it from that with red color.

Claims (1)

PATENTANSPRUCH: Verfahren zur Darstellung von Küpenfarbstoffen, darin bestehend, daß man die aus Benzanthronylpyrazolanthronen durch Kondensation erhältlichen Farbstoffe mit nitrierenden Mitteln behandelt und die erhaltenen Körper gegebenenfalls reduziert.PATENT CLAIM: Process for the representation of vat dyes, therein consisting that one obtainable from benzanthronylpyrazole anthrones by condensation Dyes treated with nitrating agents and the bodies obtained if necessary reduced.
DEI29597D 1926-11-24 1926-11-24 Process for the preparation of Kuepen dyes Expired DE492275C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEI29597D DE492275C (en) 1926-11-24 1926-11-24 Process for the preparation of Kuepen dyes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEI29597D DE492275C (en) 1926-11-24 1926-11-24 Process for the preparation of Kuepen dyes

Publications (1)

Publication Number Publication Date
DE492275C true DE492275C (en) 1930-02-24

Family

ID=7187359

Family Applications (1)

Application Number Title Priority Date Filing Date
DEI29597D Expired DE492275C (en) 1926-11-24 1926-11-24 Process for the preparation of Kuepen dyes

Country Status (1)

Country Link
DE (1) DE492275C (en)

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