DE409280C - Process for the preparation of monoazo dyes for wool - Google Patents

Process for the preparation of monoazo dyes for wool

Info

Publication number
DE409280C
DE409280C DEF51649D DEF0051649D DE409280C DE 409280 C DE409280 C DE 409280C DE F51649 D DEF51649 D DE F51649D DE F0051649 D DEF0051649 D DE F0051649D DE 409280 C DE409280 C DE 409280C
Authority
DE
Germany
Prior art keywords
wool
preparation
weight
monoazo dyes
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
DEF51649D
Other languages
German (de)
Inventor
Dr Heinrich Clingestein
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.)
Bayer AG
Original Assignee
Farbenfabriken Vorm Friedr Bayer and Co
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 Farbenfabriken Vorm Friedr Bayer and Co filed Critical Farbenfabriken Vorm Friedr Bayer and Co
Priority to DEF51649D priority Critical patent/DE409280C/en
Application granted granted Critical
Publication of DE409280C publication Critical patent/DE409280C/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
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/24Monoazo dyes prepared by diazotising and coupling from coupling components containing both hydroxyl and amino directing groups
    • C09B29/28Amino naphthols
    • C09B29/30Amino naphtholsulfonic acid

Landscapes

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

Description

Verfahren zur Darstellung von blonoazofarbstoffen für Wolle. Es wurde gefunden, daß wertvolle Wollfarbstoffe dadurch erhalten werden, daß man Diazoverbindungen der Benzolreihe, die eine Alk-vlacet laminogruppe enthalten, mit Aryly b aininonaphtholstilfosätiren und ihrenDerivaten kuppelt.Process for the preparation of blonoazo dyes for wool. It has been found that valuable wool dyes are obtained by reacting diazo compounds of the benzene series, which contain a vlacet Alk-laminogruppe, aininonaphtholstilfosätiren with Aryly b and coupling their derivatives.

Die so erhältlichen Farbstoffe sind dadurch besonders wertvoll, daß sie gut egalisieren, sehr leicht löslich sind und trotz ihrer leichten Löslichkeit gute Walkechtheit zeigen.The dyes obtainable in this way are particularly valuable in that they level well, are very easily soluble and despite their easy solubility show good flexing fastness.

Beispiel i.Example i.

17,8 Gewichtsteile p-Ai-ninoät-hylacetan#ilid iverden, wie üblich, diazotiert und die Diazoverbindung zu einer sodaalkalischen Lösung Von 35 Gewichtsteilen o-Methoxyphenyl-2-amino-8-naphthol-6-stilfosätire (iooprozentig) gegeben.17.8 parts by weight of p-aminoeth-hylacetanilide are diazotized, as usual, and the diazo compound is added to a soda-alkaline solution of 35 parts by weight of o-methoxyphenyl-2-amino-8-naphthol-6-stilfosätire (10%).

Der ausgesalzene Farbstoff färbt Wolle in braunen Tönen an.The salted-out dye stains wool in brown tones.

Beispiel 19,2 Gewichtsteile 2-Äthylacetylamiilo-4-toluidiii werden, wie üblich, diazotiert und die Diazoverbindung zu einer sodaalkalischen Lösung von 32 Gewichtsteilen Phenyl-2-amino-8-naphtliol-6-stilfosätire (iooprozentig) gegeben.Example 1 9.2 parts by weight of 2-ethylacetylamiilo-4-toluidiii are diazotized as usual and the diazo compound is added to an alkaline soda solution of 32 parts by weight of phenyl-2-amino-8-naphthol-6-stilfosätire (10%).

Der ausgesalzene Farbstoff färbt Wolle braun an. Beispiel 3. The salted-out dye stains wool brown. Example 3.

19,2 Gewichtsteile 5-Äthylacetylainino-2-toluidin werden, wie üblich, diazotiert und die Diazoverbindung zu einer sodaallzalischen Lösung von 4o Gewichtsteilen p-Ätliylacetyl--irninophenyl-2-amiiio-S-naphtliol-6-stilfosätire (iooprozentig) gegeben.19.2 parts by weight of 5-Äthylacetylainino-2-toluidine are, as usual, diazotized and the diazo compound to a sodaallzalischen solution of 40 parts by weight p-Ätliylacetyl - iminophenyl-2-amiiio-S-naphthiol-6-stilfosätire (100 percent) given.

Der ausgesalzene Farbstoff färbt Wolle in Bordeauxtönen an.The salted-out dye stains wool in shades of Bordeaux.

Beispiel 4, 19,2 Gewichtsteile 4-Äthylacetylamilioo-toluidin werden, wie üblich, diazotiert und die Diazoverbindung zu einer sodaalkalischen Lösung von 35 Gewichtsteilen p-Methoxyphenyl-2-amino-8-naphthol-6-stilfosäure (iooprozentig) gegeben.Example 4, 19.2 parts by weight of 4-ethylacetylamilio-toluidine are diazotized as usual and the diazo compound is added to an alkaline soda solution of 35 parts by weight of p-methoxyphenyl-2-amino-8-naphthol-6-stilfonic acid (10%).

Der ausgesalzene Farbstoff färbt Wolle ge g lbstichigbraun an.The salted-out dye stains wool in a yellowish brown.

Claims (1)

PATETXT-AixSPRUCH: Verfahren zur Darstellung von Monoazofarbstoffen für Wolle, dadurch gekennzeichnet, daß man diazotierte Aminoverbindungen der Benzolreihe, die eine Alkylacetylaininogruppe enthalten, mit Arylaminonaphtholsulfosäuren und ihren Derivaten vereinigt.PATETXT-AixSPRUCH: Process for the representation of monoazo dyes for wool, characterized in that diazotized amino compounds of the benzene series, which contain an alkylacetylaininogruppe with Arylaminonaphtholsulfonicäuren and their derivatives combined.
DEF51649D 1922-04-26 1922-04-26 Process for the preparation of monoazo dyes for wool Expired DE409280C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEF51649D DE409280C (en) 1922-04-26 1922-04-26 Process for the preparation of monoazo dyes for wool

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF51649D DE409280C (en) 1922-04-26 1922-04-26 Process for the preparation of monoazo dyes for wool

Publications (1)

Publication Number Publication Date
DE409280C true DE409280C (en) 1925-01-31

Family

ID=7104785

Family Applications (1)

Application Number Title Priority Date Filing Date
DEF51649D Expired DE409280C (en) 1922-04-26 1922-04-26 Process for the preparation of monoazo dyes for wool

Country Status (1)

Country Link
DE (1) DE409280C (en)

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