DE636891C - Process for the preparation of a Kuepen dye - Google Patents

Process for the preparation of a Kuepen dye

Info

Publication number
DE636891C
DE636891C DEI47907D DEI0047907D DE636891C DE 636891 C DE636891 C DE 636891C DE I47907 D DEI47907 D DE I47907D DE I0047907 D DEI0047907 D DE I0047907D DE 636891 C DE636891 C DE 636891C
Authority
DE
Germany
Prior art keywords
dye
kuepen
preparation
chlorine
parts
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
DEI47907D
Other languages
German (de)
Inventor
Dr Erich Berthold
Dr Paul Nawiasky
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 DEI47907D priority Critical patent/DE636891C/en
Application granted granted Critical
Publication of DE636891C publication Critical patent/DE636891C/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
    • C09B5/62Cyclic imides or amidines of peri-dicarboxylic acids of the anthracene, benzanthrene, or perylene series

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Description

Verfahren zur Herstellung eines Küpenfarbstoffs ' Es wurde gefunden, daß man einen wertvollen Küpenfarbstoff erhält, wenn man Perylentetracarbonsäurediphenyl@diimi,d in Gegenwart eines Chlorüberträgers und eines organischen Lösungs- oder Verdünnungsmittels so lange mit Chlor oder chlorierend wirkenden Mitteln behandelt, bis der Trichlorabkömmling entstanden ist, der aus violettblauer Küpe pflanzliche Fasern in klaren, scharlachroten Tönen färbt. Geeignete Lösungs- oder Verdünnungsmittel sind beispielsweise Nitrobenzol und Trichlorbenzol. Als Chlorüberträger seien Jod und Schwefel genannt. Der so erhältliche Küpenfarbstoff färbt pflanzliche Fasern in außerordentlich klaren, scharlachroten Tönen von: ausgezeichneten Igehtheitseigenschaften. Er ist viel leichter verküpbar als der Ausgangsstoff. - -Beispiel i Eine Mischung von 2i,6 Teilen Perylentetracarbonsäurediphenyldiimid, das Beispielsweise durch Erhitzen von Perylentetracarbonsäureanhydrid mit Anilin erhalten werden kann, 5oo Teilen Nitrobenzol, 2 Teilen Jod und 28_Teilen Sulfurylchlorid wird 4 Stunden lang unter Rühren auf 6o bis 65° erwärmt. Dann erwärmt man noch so lange auf 8o bis 85°, bis eine entnommene Probe nur noch aus den gelbroten. Kristallen der Trichlorverbindurng besteht, die eine tief violettblaue Küpe liefert. Man läBt dann erkalten; saugt den Farbstoff ab und befreit ihn vom Lösungsmittel. Das so in guter Ausbeute und Reinheit erhaltene Trichlorperylentetracarbonsäurediphenyldiimid ist ein gelbrotes Kristallpulver, das sich mit roter Farbe und gelbroter _Fluoreszenz z in konzentrierter' Schwefelsäure löst.- Es '..färbt pflanzliche Fasern aus.tief violettblauer Küpe in außerordentlich` klafen; scharläcfiroten Tönen von ausgezeichneten Echtheitseigenschaften,. besonders guter Lichtechtheit: Beispiel 2 In eine Aufschlämmung von io,8 Teilen Perylentetracarbonsäurediphenyldiimid in roo Teilen Trichlorbenzol leitet man nach Zugabe. von i Teil Jod bei i5o bis 170' so, lange Chlor ein, bis eine entnommene Probe tief violettblau küpt. Die Aufarbeitung geschieht auf die in Beispiel r angegebene Weise. Der so erhaltene Farbstoff hat dieselben Eigenschaften wie der nach Beispiel -i erhältliche.Process for preparing a vat dye It has been found that a valuable vat dye is obtained by using perylenetetracarboxylic acid diphenyl @ diimi, i.e., perylenetetracarboxylic acid diphenyl @ diimi treated with chlorine or chlorinating agents in the presence of a chlorine carrier and an organic solvent or diluent until the trichloro derivative is formed, which dyes vegetable fibers in clear, scarlet shades from a violet-blue vat. Suitable solvents or diluents are, for example, nitrobenzene and trichlorobenzene. Iodine and sulfur are mentioned as chlorine carriers. The vat dye obtainable in this way dyes vegetable fibers in extraordinarily clear, scarlet shades with excellent properties. It is much easier to connect than the starting material. Example i A mixture of 2i, 6 parts of perylenetetracarboxylic acid diphenyldiimide, which can be obtained, for example, by heating perylenetetracarboxylic anhydride with aniline, 500 parts of nitrobenzene, 2 parts of iodine and 28 parts of sulfuryl chloride is heated to 6o to 65 ° for 4 hours with stirring. Then it is heated to 8o to 85 ° until a sample taken is only from the yellow-red one. Crystals of the trichloro compound, which provides a deep violet-blue vat. You then let it cool down; sucks off the dye and frees it from the solvent. The trichloroperylenetetracarboxylic acid diphenyldiimide obtained in this way in good yield and purity is a yellow-red crystal powder which, with a red color and yellow-red fluorescence, dissolves in concentrated 'sulfuric acid. Sharp-red tones with excellent fastness properties. particularly good lightfastness: EXAMPLE 2 After addition, 10.8 parts of perylenetetracarboxylic acid diphenyldiimide in roo parts of trichlorobenzene are passed into a slurry. of i part iodine at 150 to 170 minutes in chlorine until a sample taken turns deep violet-blue. The work-up takes place in the manner indicated in example r. The dye thus obtained has the same properties as that obtainable according to Example -i.

Claims (1)

PATENTANSPRUCH -Verfahren zur Herstellung eines Küpenfarbstoffs; dadurch gekennzeichnet, daß man Perylentetracarbonsäurediphenyldiimid in Gegenwart eines Chlorüberträgers und eines organischen Lösungs- oder Verdünnungsmittels so lange mit Chlor oder chlorierend wirkenden Mitteln behandelt, bis der Trichlorabkömmling entstanden ist.PATENT CLAIM - Process for the production of a vat dye; through this characterized in that one Perylenetetracarbonsäurediphenyldiimid in the presence of a Chlorine carrier and an organic solvent or diluent for so long treated with chlorine or chlorinating agents until the trichloro derivative originated.
DEI47907D 1933-09-09 1933-09-09 Process for the preparation of a Kuepen dye Expired DE636891C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEI47907D DE636891C (en) 1933-09-09 1933-09-09 Process for the preparation of a Kuepen dye

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEI47907D DE636891C (en) 1933-09-09 1933-09-09 Process for the preparation of a Kuepen dye

Publications (1)

Publication Number Publication Date
DE636891C true DE636891C (en) 1936-10-16

Family

ID=7192115

Family Applications (1)

Application Number Title Priority Date Filing Date
DEI47907D Expired DE636891C (en) 1933-09-09 1933-09-09 Process for the preparation of a Kuepen dye

Country Status (1)

Country Link
DE (1) DE636891C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001092420A2 (en) * 2000-05-29 2001-12-06 Radiant Color N.V. Perylene dyes with persistent fluorescence caused by steric inhibition of aggregation

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001092420A2 (en) * 2000-05-29 2001-12-06 Radiant Color N.V. Perylene dyes with persistent fluorescence caused by steric inhibition of aggregation
WO2001092420A3 (en) * 2000-05-29 2002-06-20 Radiant Color N V Perylene dyes with persistent fluorescence caused by steric inhibition of aggregation

Similar Documents

Publication Publication Date Title
DE636891C (en) Process for the preparation of a Kuepen dye
DE2500237C2 (en) ANTHRACHINOID DISPERSION COLORS, THEIR PRODUCTION AND THEIR USE
DE478738C (en) Process for the production of orange dyes
DE745465C (en) Process for the preparation of phthalocyanine dyes
DE504016C (en) Process for the production of Kuepen dyes of the benzanthrone series
DE560236C (en) Process for the preparation of haloanthraquinone-2íñ1-benzacridones
DE615535C (en) Process for the production of Kuepen dyes
DE638837C (en) Process for the preparation of haloamino-1, 9-anthrapyrimidines
DE500323C (en) Process for the preparation of orange bower colors
DE436888C (en) Process for the preparation of isodibenzanthrones
DE576131C (en) Process for the preparation of Kuepen dyes of the 1,2-benzanthraquinone series
CH176928A (en) Process for the production of a vat dye.
DE622173C (en) Process for the production of Kuepen dyes
DE598779C (en) Process for the representation of dyes
DE598327C (en) Process for the production of Kuepen dyes
DE844777C (en) Process for the production of Kuepen dyes
DE525331C (en) Process for the production of new Kuepen dyes
DE865907C (en) Process for the preparation of 2'íñ4 'and 2'íñ6'-Dinitroanilinoanthraquinones
AT166701B (en) Process for the production of new vat dyes
DE607944C (en) Process for the production of nitrogen-containing condensation products
DE630220C (en) Process for the production of capsules of the anthraquinone series
DE628229C (en) Process for the production of chlorine-containing dyes
DE639378C (en) Process for the preparation of haloamino-1, 9-anthrapyrimidines
DE516784C (en) Process for the preparation of Kuepen dyes of the 1íñ2-Benzanthraquinone series
DE572977C (en) Process for the preparation of condensation products