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DE1210506B - Process for the preparation of dyes which are derived from phthalocyanines containing aryl groups - Google Patents

Process for the preparation of dyes which are derived from phthalocyanines containing aryl groups

Info

Publication number
DE1210506B
DE1210506B DEB71437A DEB0071437A DE1210506B DE 1210506 B DE1210506 B DE 1210506B DE B71437 A DEB71437 A DE B71437A DE B0071437 A DEB0071437 A DE B0071437A DE 1210506 B DE1210506 B DE 1210506B
Authority
DE
Germany
Prior art keywords
dyes
preparation
aryl groups
sulfonic acid
derived
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.)
Pending
Application number
DEB71437A
Other languages
German (de)
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.)
BASF SE
Original Assignee
BASF SE
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 BASF SE filed Critical BASF SE
Priority to DEB71437A priority Critical patent/DE1210506B/en
Publication of DE1210506B publication Critical patent/DE1210506B/en
Pending 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
    • C09B47/00Porphines; Azaporphines
    • C09B47/04Phthalocyanines abbreviation: Pc
    • C09B47/08Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
    • 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
    • C09B62/00Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/44Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
    • C09B62/523Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring the reactive group being an esterified or non-esterified hydroxyalkyl sulfonyl amido or hydroxyalkyl amino sulfonyl group, a quaternised or non-quaternised amino alkyl sulfonyl amido group, or a substituted alkyl amino sulfonyl group, or a halogen alkyl sulfonyl amido or halogen alkyl amino sulfonyl group or a vinyl sulfonylamido or a substituted vinyl sulfonamido group
    • C09B62/537Porphines; Azaporphines

Landscapes

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

Description

Verfahren zur Herstellung von Farbstoffen, die sich von Arylgruppen enthaltenden Phthalocyaninen ableiten Es wurde gefunden, daß man bei der Umsetzung von Sulfonsäurechloriden von Arylgruppen enthaltenden Phthalocyaninen, wie Tetraphenylkupferphthalocyaninsulfonsäurechloriden, mit weniger als 1 Mol eines primären oder sekundären Aminoalkylhalogenids je Sulfonsäurechloridgruppe in Gegenwart von säurebindenden Mitteln neue, wasserlösliche Farbstoffe erhält. Diese Farbstoffe enthalten (N-Halogen-alkyl)-sulfonamidgruppen.Process for the preparation of dyes that differ from aryl groups Derive containing phthalocyanines It has been found that the reaction of sulfonic acid chlorides of phthalocyanines containing aryl groups, such as tetraphenyl copper phthalocyanine sulfonic acid chlorides, with less than 1 mole of a primary or secondary aminoalkyl halide per sulfonic acid chloride group receives new, water-soluble dyes in the presence of acid-binding agents. These dyes contain (N-halo-alkyl) sulfonamide groups.

Die verwendeten Arylgruppen enthaltenden Phthalocyanine sollen zwei, vorzugsweise drei oder vier Sulfonsäurechloridgruppen je Farbstoffmolekül enthalten.The aryl group-containing phthalocyanines used should be two, preferably contain three or four sulfonic acid chloride groups per dye molecule.

Als Halogenalkylamine können sowohl primäre als auch sekundäre aliphatische Amine verwendet werden, insbesondere solche primären Amine, bei denen sich das Halogenatom und die Aminogruppe an zwei benachbarten Kohlenstoffatomen befinden, wie Chlor-Bromäthylamin, ß - Chlorisopropylamin, 1 - Chlor-2-aminobutan und 2-Chlor-3-aminobutan.Both primary and secondary aliphatic amines can be used as haloalkylamines Amines are used, especially those primary amines in which the halogen atom and the amino group is on two adjacent carbon atoms, such as chloro-bromoethylamine, ß - chloroisopropylamine, 1 - chloro-2-aminobutane and 2-chloro-3-aminobutane.

Man verwendet die Aminoalkylhalogenide vorteilhaft in Form ihrer halogenwasserstoffsauren Salze. Man nimmt für die Umsetzung im allgemeinen nur so viel Amin, daß zwei Drittel bis ein Drittel der Sulfonsäurechloridgruppen in Sulfonamidgruppen übergeführt werden, jedenfalls weniger als 1 Mol Amin je Sulfonsäurechloridgruppe, und arbeitet in Gegenwart von säurebindenden Mitteln, z. B. Alkalihydroxyden, Alkalicarbonaten oder Alkaliacetaten, oder tertiären Aminen, wie Pyridin. Die Umsetzung kann in wäßriger Flüssigkeit vorgenommen werden, wobei gleichzeitig der nicht umgesetzte Sulfonsäurechloridrest verseift wird. Man trennt die Farbstoffe aus den wäßrigen Lösungen ab durch Zugabe von Salzen oder von Säuren.The aminoalkyl halides are advantageously used in the form of their hydrohalic acids Salts. In general, only so much amine is used for the reaction that two thirds until one third of the sulfonic acid chloride groups are converted into sulfonamide groups, in any case less than 1 mole of amine per sulfonic acid chloride group, and works in the presence of acid-binding agents, e.g. B. alkali hydroxides, alkali carbonates or alkali acetates, or tertiary amines such as pyridine. The reaction can be carried out in an aqueous liquid at the same time the unreacted sulfonic acid chloride residue is saponified will. The dyes are separated from the aqueous solutions by adding salts or from acids.

Die so erhältlichen, Arylgruppen enthaltenden Phthalocyanine, die neben Halogenalkylsulfonamidgruppen noch wesentliche Mengen freier Sulfonsäuregruppen enthalten, sind in Wasser löslich und liefern auf Baumwolle wasch- und sodakochechte Färbungen. Sie sind den entsprechenden Farbstoffen, die durch Umsetzung von mindestens molaren oder noch größeren Mengen Amin je Sulfonsäurechloridgruppe enthalten werden, sowohl in der Löslichkeit als auch in der Wasch- und Sodakochechtheit der damit auf Baumwolle erzielbaren Färbungen weitgehend überlegen. Die in dem folgenden Beispiel genannten Teile sind Gewichtsteile.The aryl group-containing phthalocyanines obtainable in this way, the In addition to haloalkylsulphonamide groups, there are also substantial amounts of free sulphonic acid groups are soluble in water and are washable and soda-proof on cotton Colorations. They are the corresponding dyes that are produced by implementing at least molar or even larger amounts of amine are contained per sulfonic acid chloride group, both in the solubility and in the fastness to washing and soda cooking Largely superior to the dyeings that can be achieved on cotton. The ones in the following example parts mentioned are parts by weight.

Beispiel 50 Teile Tetraphenylkupferphthalocyanin werden in 400 Teilen Chlorsulfonsäure 21/2 Stunden auf 130°C erwärmt. Nach dem Erkalten gießt man auf Eis, saugt ab und wäscht so lange mit kaltem Wasser, bis das Waschwasser sich schwach grün färbt. Dann teigt man den Filterrückstand, ein sulfochloriertes Tetraphenylkupferphthalocyanin, mit Wasser und Eis an, gibt eine Lösung von 15 Teilen Chloräthylaminhydrochlorid in 50 Teilen Wasser hinzu und trägt unter Rühren 200 Teile einer 10 °/oigen Natriumhydroxydlösung ein. Nach etwa 12 Stunden fällt man mit verdünnter Säure, saugt ab und trocknet. Man erhält so ein wasserlösliches Derivat des Tetraphenylkupferphthalocyanins, das Chloräthylsulfonamid- und freie Sulfonsäuregruppen enthält. Der Farbstoff färbt Baumwolle in grünen Tönen.Example 50 parts of tetraphenyl copper phthalocyanine are in 400 parts Chlorosulfonic acid heated to 130 ° C for 21/2 hours. After cooling, you pour on Ice, sucks off and washes with cold water until the wash water turns weak colors green. Then you paste the filter residue, a sulfochlorinated tetraphenyl copper phthalocyanine, with water and ice, there is a solution of 15 parts of chloroethylamine hydrochloride in 50 parts of water and carry 200 parts of a 10% sodium hydroxide solution with stirring a. After about 12 hours, it is precipitated with dilute acid, filtered off with suction and dried. A water-soluble derivative of tetraphenyl copper phthalocyanine is obtained in this way Contains chloroethylsulphonamide and free sulphonic acid groups. The dye stains Cotton in green tones.

Claims (1)

Patentanspruch: Verfahren zur Herstellung von Farbstoffen, die sich von Arylgruppen enthaltenden Phthalocyaninen ableiten, dadurch gekennzeichnet, daß man Sulfonsäurechloride von Arylgruppen enthaltenden Kupferphthalocyaninen mit weniger als 1 Mol eines primären oder sekundären Aminoalkylhalogenids je Sulfonsäurechloridgruppe in Gegenwart von säurebindenden Mitteln umsetzt. In Betracht gezogene Druckschriften: Französische Patentschrift Nr. 1117 562. Bei der Bekanntmachung der Anmeldung ist eine mit Erläuterungen versehene Färbetafel ausgelegt worden.Claim: A process for the preparation of dyes derived from phthalocyanines containing aryl groups, characterized in that sulfonic acid chlorides of aryl group-containing copper phthalocyanines are reacted with less than 1 mol of a primary or secondary aminoalkyl halide per sulfonic acid chloride group in the presence of acid-binding agents. Documents considered: French patent specification No. 1117 562. When the application was published, an explanatory coloring table was laid out.
DEB71437A 1957-07-06 1957-07-06 Process for the preparation of dyes which are derived from phthalocyanines containing aryl groups Pending DE1210506B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEB71437A DE1210506B (en) 1957-07-06 1957-07-06 Process for the preparation of dyes which are derived from phthalocyanines containing aryl groups

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB71437A DE1210506B (en) 1957-07-06 1957-07-06 Process for the preparation of dyes which are derived from phthalocyanines containing aryl groups

Publications (1)

Publication Number Publication Date
DE1210506B true DE1210506B (en) 1966-02-10

Family

ID=6977040

Family Applications (1)

Application Number Title Priority Date Filing Date
DEB71437A Pending DE1210506B (en) 1957-07-06 1957-07-06 Process for the preparation of dyes which are derived from phthalocyanines containing aryl groups

Country Status (1)

Country Link
DE (1) DE1210506B (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1117562A (en) * 1953-12-21 1956-05-24 Bayer Ag New basic dyes and their production process

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1117562A (en) * 1953-12-21 1956-05-24 Bayer Ag New basic dyes and their production process

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