DE1148341B - Verfahren zur Herstellung von Farbstoffen - Google Patents

Verfahren zur Herstellung von Farbstoffen

Info

Publication number
DE1148341B
DE1148341B DEG26911A DEG0026911A DE1148341B DE 1148341 B DE1148341 B DE 1148341B DE G26911 A DEG26911 A DE G26911A DE G0026911 A DEG0026911 A DE G0026911A DE 1148341 B DE1148341 B DE 1148341B
Authority
DE
Germany
Prior art keywords
parts
dye
anthraquinone
dyes
radical
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
DEG26911A
Other languages
German (de)
English (en)
Inventor
Dr Hans-Rudolf Schwander
Dr Jean-Pierre Jung
Dr Peter Hindermann
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.)
Novartis AG
Original Assignee
JR Geigy 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 JR Geigy AG filed Critical JR Geigy AG
Publication of DE1148341B publication Critical patent/DE1148341B/de
Pending legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
    • C09B5/02—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position
    • C09B5/16—Benz-diazabenzanthrones, e.g. anthrapyrimidones
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16—Amino-anthraquinones
    • C09B1/20—Preparation from starting materials already containing the anthracene nucleus
    • C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
    • C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
    • C09B1/34—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16—Amino-anthraquinones
    • C09B1/20—Preparation from starting materials already containing the anthracene nucleus
    • C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
    • C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
    • C09B1/34—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated
    • C09B1/343—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated only sulfonated in the anthracene nucleus
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16—Amino-anthraquinones
    • C09B1/20—Preparation from starting materials already containing the anthracene nucleus
    • C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
    • C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
    • C09B1/34—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated
    • C09B1/346—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated only sulfonated in a substituent
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/50—Amino-hydroxy-anthraquinones; Ethers and esters thereof
    • C09B1/54—Amino-hydroxy-anthraquinones; Ethers and esters thereof etherified
    • C09B1/547—Anthraquinones with aromatic ether groups
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/44—Reactive 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
    • C09B62/465—Reactive 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 acryloyl group, a quaternised or non-quaternised aminoalkyl carbonyl group or a (—N)n—CO—A—O—X or (—N)n—CO—A—Hal group, wherein A is an alkylene or alkylidene group, X is hydrogen or an acyl radical of an organic or inorganic acid, Hal is a halogen atom, and n is 0 or 1
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/44—Reactive 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
    • C09B62/465—Reactive 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 acryloyl group, a quaternised or non-quaternised aminoalkyl carbonyl group or a (—N)n—CO—A—O—X or (—N)n—CO—A—Hal group, wherein A is an alkylene or alkylidene group, X is hydrogen or an acyl radical of an organic or inorganic acid, Hal is a halogen atom, and n is 0 or 1
    • C09B62/467—Anthracene dyes
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
    • Y10S8/916—Natural fiber dyeing
    • Y10S8/917—Wool or silk

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
DEG26911A 1958-04-23 1959-04-22 Verfahren zur Herstellung von Farbstoffen Pending DE1148341B (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH5866458A CH389127A (de) 1958-04-23 1958-04-23 Verfahren zur Herstellung von Farbstoffen

Publications (1)

Publication Number Publication Date
DE1148341B true DE1148341B (de) 1963-05-09

Family

ID=4521840

Family Applications (2)

Application Number Title Priority Date Filing Date
DEG31650A Pending DE1154212B (de) 1958-04-23 1959-04-22 Verfahren zur Herstellung von Anthrachinonfarbstoffen
DEG26911A Pending DE1148341B (de) 1958-04-23 1959-04-22 Verfahren zur Herstellung von Farbstoffen

Family Applications Before (1)

Application Number Title Priority Date Filing Date
DEG31650A Pending DE1154212B (de) 1958-04-23 1959-04-22 Verfahren zur Herstellung von Anthrachinonfarbstoffen

Country Status (8)

Country Link
US (1) US3376320A (US07582779-20090901-C00044.png)
BE (1) BE577990A (US07582779-20090901-C00044.png)
CH (1) CH389127A (US07582779-20090901-C00044.png)
DE (2) DE1154212B (US07582779-20090901-C00044.png)
ES (1) ES248867A1 (US07582779-20090901-C00044.png)
FR (1) FR1222194A (US07582779-20090901-C00044.png)
GB (1) GB903590A (US07582779-20090901-C00044.png)
NL (2) NL121734C (US07582779-20090901-C00044.png)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1644544B1 (de) * 1965-03-03 1971-12-02 Ciba Geigy Ag Saure Anthrachinonfarbstoffgemische,deren Herstellung und Verwendung

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL121826C (US07582779-20090901-C00044.png) * 1959-07-24
CH414041A (de) * 1960-09-12 1966-05-31 Sandoz Ag Verfahren zur Herstellung von Reaktivfarbstoffen
DE1180082B (de) * 1961-09-01 1964-10-22 Sandoz Ag Verfahren zur Herstellung von Reaktiv-farbstoffen der Anthrachinonreihe
DE1264647B (de) * 1961-09-23 1968-03-28 Bayer Ag Verfahren zur Herstellung von Anthrachinonfarbstoffen
DE1253842B (de) * 1962-01-10 1967-11-09 Sandoz Ag Verfahren zur Herstellung von Anthrachinonfarbstoffen
FR89558E (US07582779-20090901-C00044.png) * 1963-02-18
US3492319A (en) * 1966-06-21 1970-01-27 Gaf Corp Quaternary anthraquinone dyestuffs
DE2305206C2 (de) * 1972-02-04 1984-09-06 Ciba-Geigy Ag, Basel Faserreaktive Anthrachinonverbindungen, Verfahren zu deren Herstellung und ihre Verwendung
DE3142852A1 (de) * 1981-10-29 1983-05-11 Bayer Ag, 5090 Leverkusen Anthrachinon-reaktivfarbstoffe, verfahren zu ihrer herstellung und ihre verwendung zum faerben und bedrucken von stickstoffhaltigen materialien
US4693727A (en) * 1984-11-08 1987-09-15 Ciba-Geigy Corporation Process for dyeing synthetic polyamide materials with fibre-reactive anthraquinone dyes
US4652269A (en) * 1984-11-08 1987-03-24 Ciba-Geigy Corporation Process for the continuous trichromatic dyeing of synthetic polyamide materials: including a blue anthraquinone reactive dye
EP0601970A1 (de) * 1992-12-03 1994-06-15 Ciba-Geigy Ag Anthrachinonfarbstoffe, Verfahren zu deren Herstellung und deren Verwendung
DE59408676D1 (de) 1993-05-18 1999-10-07 Ciba Sc Holding Ag Farbstoffmischungen, 1:2-Kobaltkomplexformazanfarbstoffe und deren Verwendung
US6551364B2 (en) 1993-05-18 2003-04-22 Ciba Specialty Chemicals Corporation Dye mixtures, 1:2 cobalt complex formazan dyes and their use
EP0718374B1 (de) 1994-12-21 2002-03-06 Ciba SC Holding AG 1:2-Chromkomplexfarbstoffe enthaltende Farbstoffmischungen und 1:2 Chromkomplexfarbstoffe
CN101538417B (zh) * 2008-12-12 2012-12-05 天津德凯化工股份有限公司 一种制备酸性蓝260的方法
WO2013051724A1 (en) * 2011-10-04 2013-04-11 Canon Kabushiki Kaisha Water-insoluble coloring matter compound, ink using the water-insoluble coloring matter compound, thermal transfer recording sheet and resist composition for color filter
CN112457684B (zh) * 2020-12-24 2022-12-06 北京泛博化学股份有限公司 一种毛皮用酸性红染料及其制备方法和应用

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1927125A (en) * 1929-07-17 1933-09-19 Gen Aniline Works Inc Acid wool-dyestuff of the anthraquionone series and process of making same
DE1016230B (de) * 1953-12-15 1957-09-26 Ciba Geigy Verfahren zur Herstellung echter Faerbungen

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2029007A (en) * 1936-01-28 xcoxch
US2117569A (en) * 1936-06-18 1938-05-17 Firm Chemical Works Formerly S Dyestuffs of the anthraquinone series and a process for their manufacture
US2419405A (en) * 1943-05-05 1947-04-22 Du Pont Process for preparing 1-hydroxy-4-arylamino anthraquinones
US2659737A (en) * 1950-12-08 1953-11-17 Peter Albin Dyestuff intermediates of the anthraquinone series
CH317121A (de) * 1952-04-18 1956-11-15 Bayer Ag Verfahren zur Herstellung von sauren Wollfarbstoffen der Anthrachinonreihe
NL94555C (US07582779-20090901-C00044.png) * 1954-12-31

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1927125A (en) * 1929-07-17 1933-09-19 Gen Aniline Works Inc Acid wool-dyestuff of the anthraquionone series and process of making same
DE1016230B (de) * 1953-12-15 1957-09-26 Ciba Geigy Verfahren zur Herstellung echter Faerbungen

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1644544B1 (de) * 1965-03-03 1971-12-02 Ciba Geigy Ag Saure Anthrachinonfarbstoffgemische,deren Herstellung und Verwendung

Also Published As

Publication number Publication date
CH389127A (de) 1965-03-15
NL121734C (US07582779-20090901-C00044.png) 1966-12-16
FR1222194A (fr) 1960-06-08
ES248867A1 (es) 1960-01-01
BE577990A (fr) 1959-10-22
GB903590A (en) 1962-08-15
US3376320A (en) 1968-04-02
DE1154212B (de) 1963-09-12
NL238454A (US07582779-20090901-C00044.png) 1964-01-27

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