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GB1095121A - Process for the production of mono-azo basic dyes - Google Patents

Process for the production of mono-azo basic dyes

Info

Publication number
GB1095121A
GB1095121A GB41165A GB41165A GB1095121A GB 1095121 A GB1095121 A GB 1095121A GB 41165 A GB41165 A GB 41165A GB 41165 A GB41165 A GB 41165A GB 1095121 A GB1095121 A GB 1095121A
Authority
GB
United Kingdom
Prior art keywords
mono
group
alkylsulphenyl
formula
alkylaminosulphonyl
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
GB41165A
Inventor
Roland Entschel
Curt Muller
Walter Wehrli
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.)
WESTMINSTER BANK Ltd
Original Assignee
WESTMINSTER BANK Ltd
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
Priority claimed from CH489862A external-priority patent/CH496765A/en
Priority claimed from CH470961A external-priority patent/CH435495A/en
Priority claimed from CH35962A external-priority patent/CH462348A/en
Priority claimed from CH1501362A external-priority patent/CH461664A/en
Application filed by WESTMINSTER BANK Ltd filed Critical WESTMINSTER BANK Ltd
Publication of GB1095121A publication Critical patent/GB1095121A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/22—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with hetero atoms directly attached to ring nitrogen atoms
    • C07D295/28—Nitrogen atoms
    • C07D295/30—Nitrogen atoms non-acylated
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/0041—Optical brightening agents, organic pigments
    • 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
    • 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
    • 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
    • C09B1/51—N-substituted amino-hydroxy anthraquinone
    • 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
    • C09B1/542—Anthraquinones with aliphatic, cycloaliphatic, araliphatic or 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
    • C09B44/00—Azo dyes containing onium groups
    • C09B44/02—Azo dyes containing onium groups containing ammonium groups not directly attached to an azo group
    • C09B44/04—Azo dyes containing onium groups containing ammonium groups not directly attached to an azo group from coupling components containing amino as the only directing group
    • 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
    • C09B62/62—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 ethylenimino or N—acylated ethylenimino group or a —CO—NH—CH2—CH2—X group, wherein X is a halogen atom, a quaternary ammonium group or O—acyl and acyl is derived from an organic or inorganic acid, or a beta—substituted ethylamine group
    • C09B62/66—Azo dyes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Coloring (AREA)
  • Treatment Of Fiber Materials (AREA)

Abstract

Basic mono-azo dyes of formula <FORM:1095121/C4-C5/1> in which R9 is Cl, Br or CN or an alkylsulphenyl, mono- or di-alkylaminosulphonyl group, R11 is H, Cl, Br or NO2 or a -CO-alkyl, alkylsulphenyl, mono- or di-alkylaminosulphonyl group, R12 is H, Cl, CN or an alkylsulphenyl, mono- or di-alkylaminosulphonyl group, R13 is H, Cl, Br or NO2, R18 is H, Cl, Br, or an alkyl group, R7 is a methyl or ethyl group, Y is -C2H4- or <FORM:1095121/C4-C5/2> is the radical <FORM:1095121/C4-C5/3> or <FORM:1095121/C4-C5/4> or together with R7 and the N atom bound to R7 and Y the radical <FORM:1095121/C4-C5/5> X- is an anion provided that R11 shall not represent NO2 when one of the radicals R9 or R13 is chlorine, Y is -C2H4- and K is as above, are prepared by coupling one mole of a diazo compound of an amine of formula <FORM:1095121/C4-C5/6> with 1 mole of a compound of formula <FORM:1095121/C4-C5/7> all symbols being as above. The dyes are particularly useful for dyeing polyacrylonitrile and its co-polymers, the dyeing being in aqueous neutral or acidic medium if desired as above atmospheric pressure. Yellow-violet shades are obtained. The Specification disclaims subject-matter in Claim 16 of Specification 1,008,636.
GB41165A 1961-04-21 1965-01-05 Process for the production of mono-azo basic dyes Expired GB1095121A (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
CH489862A CH496765A (en) 1961-04-21 1961-04-21 Basic anthraquinone dyes for polymers of - acrylonitrile and copolymers of acrylonitrile and vinyl ace
CH470961A CH435495A (en) 1961-04-21 1961-04-21 Process for the preparation of hydrazine derivatives
CH35962A CH462348A (en) 1962-01-12 1962-01-12 Process for the preparation of hydrazine derivatives
CH1501362A CH461664A (en) 1962-12-21 1962-12-21 Process for the production of hydrozine derivatives
CH47964 1964-12-15

Publications (1)

Publication Number Publication Date
GB1095121A true GB1095121A (en) 1967-12-13

Family

ID=27508806

Family Applications (1)

Application Number Title Priority Date Filing Date
GB41165A Expired GB1095121A (en) 1961-04-21 1965-01-05 Process for the production of mono-azo basic dyes

Country Status (3)

Country Link
DE (3) DE1644321C3 (en)
GB (1) GB1095121A (en)
NL (3) NL6500323A (en)

Also Published As

Publication number Publication date
DE1644321A1 (en) 1971-05-06
NL6500322A (en) 1965-07-19
DE1644321B2 (en) 1974-08-29
DE1644322B2 (en) 1974-05-22
DE1644320A1 (en) 1971-05-06
DE1644321C3 (en) 1975-04-17
DE1644320B2 (en) 1974-05-22
DE1644320C3 (en) 1975-01-02
DE1644322C3 (en) 1975-01-09
DE1644322A1 (en) 1971-05-06
NL6500323A (en) 1965-07-19
NL6500324A (en) 1965-07-19

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