DE470502C - Process for the preparation of Kuepen dyes - Google Patents

Process for the preparation of Kuepen dyes

Info

Publication number
DE470502C
DE470502C DEI29849D DEI0029849D DE470502C DE 470502 C DE470502 C DE 470502C DE I29849 D DEI29849 D DE I29849D DE I0029849 D DEI0029849 D DE I0029849D DE 470502 C DE470502 C DE 470502C
Authority
DE
Germany
Prior art keywords
preparation
parts
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
DEI29849D
Other languages
German (de)
Inventor
Dr Heinrich Neresheimer
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 DEI29849D priority Critical patent/DE470502C/en
Application granted granted Critical
Publication of DE470502C publication Critical patent/DE470502C/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
    • C09B3/40Pyranthrones
    • C09B3/44Preparation from starting materials already containing the pyranthrone nucleus

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Optical Filters (AREA)

Description

Verfahren zur Darstellung von Küpenfarbstoffen Es wurde gefunden, daß man zu neuen wertvollen Küpenfarbstoffen der Pyranthronreihe gelangt, wenn man die Bz - BZ-Diarylpyranthrone, wie sie in der Patentschrift 278 424 beschrieben sind, mit oxydierend Benutzt man nicht oxydierend wirkende Kondensationsmittel, z. B. Aluminiumchlorid, so erhält man zunächst den gleichen Körper in einer Reduktionsstufe, die sich leicht zum Farbstoff selbst oxydieren läßt. Die neuen Farbstoffe unterscheiden sich von den Bz - Bz'-Diarylpyranthronen u. a. durch einen im allgemeinen nach Rot verschobenen Farbton.Process for the preparation of vat dyes It has been found that new valuable vat dyes of the pyranthrone series are obtained if the Bz - BZ-diarylpyranthrones, as described in patent specification 278 424, are oxidized If you use non-oxidizing condensation agents, z. B. aluminum chloride, the same body is first obtained in a reduction stage which can easily be oxidized to the dye itself. The new dyes differ from the Bz - Bz'-diarylpyranthrones, inter alia, in a hue that is generally shifted towards red.

Beispiel i Eine Lösung von io Teilen Bz-Bz'-Diphenylpyranthron in iooTeilen konzentrierter Schwefelsäure wird unter guter Kühlung mit einer Suspension von 6Teilen künstlichem oder kondensierend wirkenden Mitteln behandelt. Bei Verwendung oxydierend wirkender Mittel, z. B. Mangansuperoxyd, verläuft die Reaktion im einfachsten Falle wahrscheinlich nach folgender Gleichung: BraunsteÜi von etwa 55N MnO.-Gehalt in iooTeilen konzentrierter Schwefelsäure versetzt und so lange gerührt, bis die anfangs rotstichig blaue Farbe der Lösun 'g in ein reines Grün übergegangen ist. Man gießt in Wasser, arbeitet den in vorzüglicher Ausbeute entstandenen Farbstoff in der üblichen Weise auf und reinigt ihn, wenn nötig, durch Behandlung mit Natriumhypochloritlösung. Er bildet ein rotoranges Pulver, das sich in konzentrierter Schwefelsäure mit grüner Farbe löst. Aus der grün-en alkalischen Hydros-ulfitküpe erhält man lebhafte Orangefärbungen von guter Echtheit. Beispiel 2 4o Teile Altuniniumchlorid und io Teile Kochsalz werden bei 140' geschmolzen -und in das Gemisch ioTeile Bz-Bz'-Diphenylpyranthron eingetragen. Nach kurzer Zeit hat sich die Hydroverbindung des neuen Farbstoffes g gebildet. Teilweise schon bei der Aufarbeitung durch Berührung mit der Luft geht sie völlig beim Einleiten solcher in den Farbstoff selbst über, der in seinen chemischen und färberischen Eigenschaften mit dem des Beispiels i übereinstimmt.Example i A solution of 10 parts of Bz-Bz'-diphenylpyranthrone in 100 parts of concentrated sulfuric acid is treated with a suspension of 6 parts of artificial or condensing agents while being well cooled. When using oxidizing agents such. B. Manganese peroxide, the reaction in the simplest case probably proceeds according to the following equation: BraunsteÜi of 55N MnO. content is passed into a pure green offset in iooTeilen concentrated sulfuric acid and stirred until the initially reddish blue color of the Lösun 'g approximately. It is poured into water, the dye, which has been obtained in excellent yield, is worked up in the usual manner and, if necessary, purified by treatment with sodium hypochlorite solution. It forms a red-orange powder that dissolves in concentrated sulfuric acid with a green color. The green, alkaline hydrosulfite vat gives lively orange colorations of good fastness. Example 2 40 parts of aluminum chloride and 10 parts of common salt are melted at 140 'and 10 parts of Bz-Bz'-diphenylpyranthrone are added to the mixture. After a short time, the hydro compound of the new dye g has formed. In some cases even when working up through contact with the air, it is completely transferred when such is introduced into the dye itself, the chemical and dyeing properties of which correspond to those of Example i.

Claims (1)

PATrNTANSPRUCH: Verfahren zur Darstellung von KÜpenfarbstoffen, dadurch gekennzeichnet, daß man Bz-Bz'-Diarylpyranthrone mit oxydierend oder kondensierend -wirkenden Mitteln behandelt».PATRNT CLAIM: Process for the representation of vat dyes, thereby characterized in that one Bz-Bz'-diarylpyranthrones with oxidizing or condensing -acting means treated ».
DEI29849D 1926-12-24 1926-12-24 Process for the preparation of Kuepen dyes Expired DE470502C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEI29849D DE470502C (en) 1926-12-24 1926-12-24 Process for the preparation of Kuepen dyes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEI29849D DE470502C (en) 1926-12-24 1926-12-24 Process for the preparation of Kuepen dyes

Publications (1)

Publication Number Publication Date
DE470502C true DE470502C (en) 1929-01-18

Family

ID=7187441

Family Applications (1)

Application Number Title Priority Date Filing Date
DEI29849D Expired DE470502C (en) 1926-12-24 1926-12-24 Process for the preparation of Kuepen dyes

Country Status (1)

Country Link
DE (1) DE470502C (en)

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