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DE533499C - Process for the preparation of new Kuepen dyes - Google Patents

Process for the preparation of new Kuepen dyes

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Publication number
DE533499C
DE533499C DE1930533499D DE533499DD DE533499C DE 533499 C DE533499 C DE 533499C DE 1930533499 D DE1930533499 D DE 1930533499D DE 533499D D DE533499D D DE 533499DD DE 533499 C DE533499 C DE 533499C
Authority
DE
Germany
Prior art keywords
preparation
new
dyes
kuepen dyes
kuepen
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
DE1930533499D
Other languages
German (de)
Inventor
Dr Oskar Unger
Dr Anton Vilsmeier
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
Application granted granted Critical
Publication of DE533499C publication Critical patent/DE533499C/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Coloring (AREA)

Description

Verfahren zur Darstellung neuer Küpenfarbstoffe Die durch Verschmelzen von Benzanthron und seinen Derivaten mit Ätzalkalien entstehenden Farbstoffe der Dibenzanthron- und Isodibenzanthronreihe besitzen, soweit sie violette Küpenfarbstoffe .darstellen, vielfach die ungünstige Eigenschaft, daß ihre Färbungen beim Bettipfen mit Wasser einen mehr oder minder starken Umschlag der Nuance von Violett nach Rot zeigen.Process for the preparation of new vat dyes Die by fusing dyes formed from benzanthrone and its derivatives with caustic alkalis Dibenzanthrone and isodibenzanthrone series, as far as they have purple vat dyes .represent, in many cases, the unfavorable property that their colorations in Bettipfen with water a more or less strong change of the shade from violet to red demonstrate.

Es wurde nun gefunden, daß man neue Küpenfarbstoffe, die wahrscheinlich der Dibenzanthron- oder Isodibenzanthronreihe angehören, erhalten kann, deren Ausfärbungen auf Baumwolle beim Betupfen mit Wasser praldisch keinen Umschlag zeigen, #venn man die aus :2-Dialkylaminoanthrachinonen in der Üblichen Weise erhältlichen Benzanthrone mit alkalisch wirkenden Mitteln behandelt. B e i s p i e 1 Ein Gemisch aus 5oo Teilen go'/,igem Ätzkali und 5ooTeilen Äthylalkohol wird unter Abdestillieren des überschüssigen Al- kohols auf 170' erhitzt. Hierauf trägt man bei 15o bis 155' 5oTeile N-Dimethylaminobenzanthron vom F. 187 bis 189', erhalten durch Einwirkung von Glycerin und Eisenpulver au ' f -9-Dirnethylaminoanthrachinon in 85'/"iger Schwefelsäure, ein. Man hält einige Zeit lang bei 15o bis 16o', gießt in Wasser und gewinnt den Farbstoff durch Ausblasen mit Luft und Filtrieren. Zur Reinigung kann der Farbstoff z. B. mit Trichlorbenzol ausgekocht oder aus der schwefelsauren Lösung fraktioniert gefällt wer-den. Der reine stickstoffhaltige Farbstöff, löslich in konzentrierter Schwefelsäure mit rotvioletter Farbe, färbt aus blauer Küpe, die eine braunrote Fluoreszenz zeigt, Baumwolle in reinblauen Tönen, die beim Seifen in ein leuchtendes Blauviolett übergehen. Die erhaltene Färbung zeichnet sich durch hervorragende Wassertropfechtheit aus.It has now been found that new vat dyes, which probably belong to the dibenzanthrone or isodibenzanthrone series, can be obtained, the stains of which on cotton show no praldic change when dabbed with water, if one uses the benzanthrones obtainable in the usual way from: 2-dialkylaminoanthraquinones treated with alkaline agents. B ice p e 1 A mixture of 5oo parts go '/, potassium hydroxide and sodium 5ooTeilen ethyl alcohol while distilling off the excess Al kohols 170' is heated. Then one carries at 15o to 155 '5oTeile N-Dimethylaminobenzanthron mp 187-189', obtained by the action of glycerol and iron powder au 'f -9-Dirnethylaminoanthrachinon in 85' / "sulfuric acid, a. Is maintained for some time at long 15o to 16o ', pour into water and recover the dye by blowing out with air and filtering. For cleaning, the dye can e.g. be boiled with trichlorobenzene or fractionated from the sulfuric acid solution. The pure nitrogen-containing dye, soluble in concentrated Sulfuric acid with a red-violet color, dyes from a blue vat, which shows a brown-red fluorescence, cotton in pure blue tones, which change into a bright blue-violet when soaped.

Claims (1)

PATENTANSPRUCH: Verfahren zur Darstellung neuer Küpenfarbstoffe, I dadurch gekennzeichnet, daß man die aus 2-Dialkylaminoanthrachinonen erhältlichen Benzanthrone mit alkalisch wirkenden Mitteln behandelt.PATENT CLAIM: Process for the preparation of new vat dyes, I characterized in that one obtainable from 2-dialkylaminoanthraquinones Benzanthrones treated with alkaline agents.
DE1930533499D 1930-01-19 1930-01-19 Process for the preparation of new Kuepen dyes Expired DE533499C (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE533499T 1930-01-19

Publications (1)

Publication Number Publication Date
DE533499C true DE533499C (en) 1931-09-16

Family

ID=6556054

Family Applications (1)

Application Number Title Priority Date Filing Date
DE1930533499D Expired DE533499C (en) 1930-01-19 1930-01-19 Process for the preparation of new Kuepen dyes

Country Status (1)

Country Link
DE (1) DE533499C (en)

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