GB1244211A - Anthraquinone compounds - Google Patents

Anthraquinone compounds

Info

Publication number
GB1244211A
GB1244211A GB2598268A GB2598268A GB1244211A GB 1244211 A GB1244211 A GB 1244211A GB 2598268 A GB2598268 A GB 2598268A GB 2598268 A GB2598268 A GB 2598268A GB 1244211 A GB1244211 A GB 1244211A
Authority
GB
United Kingdom
Prior art keywords
compound
anthraquinone
rzh
reacting
red
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
GB2598268A
Inventor
Colin William Greenhalgh
Edwin Dennis Harvey
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB2598268A priority Critical patent/GB1244211A/en
Priority to BE733585D priority patent/BE733585A/xx
Priority to NL6908174A priority patent/NL6908174A/xx
Priority to DE19691927312 priority patent/DE1927312A1/en
Priority to FR6917898A priority patent/FR2009680A7/fr
Publication of GB1244211A publication Critical patent/GB1244211A/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
    • C09B1/00Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16Amino-anthraquinones
    • C09B1/20Preparation from starting materials already containing the anthracene nucleus
    • 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
    • C09B1/00Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/56Mercapto-anthraquinones
    • 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
    • C09B62/78Reactive 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 with other reactive groups
    • C09B62/80Anthracene dyes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

1,244,211. Anthraquinone compounds. IMPERIAL CHEMICAL INDUSTRIES Ltd. 29 April, 1969 [30 May, 1968], No. 25982/68. Heading C4P. The invention comprises dyestuffs of the general formula wherein Z is -O- or -S-, X is OH, or an amino group, R is a oyclohexyl radical or an alkyl radical optionally substituted by OH, alkoxy, CN, hydroxyalkoxy or aryl, and rings A and B may be further substituted e.g. by OH, halogen or sulphonamido. The preferred dyes are free from acid-water-solubilizing groups and are substituted para to X. They are prepared by reacting the corresponding 2- chloromethyl- or 2-bromomethyl-anthraquinone with a compound RZH or by reacting the corresponding 2 - methylol anthraquinone compound with a compound RZH in presence of an acid catalyst. The dyes give yellow, orange, red, red-brown and blue shades by padding, printing or dyeing on wool, silk, synthetic polyamides, polyacrylonitrile, polyesters and cellulose acetates.
GB2598268A 1968-05-30 1968-05-30 Anthraquinone compounds Expired GB1244211A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
GB2598268A GB1244211A (en) 1968-05-30 1968-05-30 Anthraquinone compounds
BE733585D BE733585A (en) 1968-05-30 1969-05-23
NL6908174A NL6908174A (en) 1968-05-30 1969-05-29
DE19691927312 DE1927312A1 (en) 1968-05-30 1969-05-29 Process for the preparation of anthraquinone dyes
FR6917898A FR2009680A7 (en) 1968-05-30 1969-05-30

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2598268A GB1244211A (en) 1968-05-30 1968-05-30 Anthraquinone compounds

Publications (1)

Publication Number Publication Date
GB1244211A true GB1244211A (en) 1971-08-25

Family

ID=10236444

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2598268A Expired GB1244211A (en) 1968-05-30 1968-05-30 Anthraquinone compounds

Country Status (5)

Country Link
BE (1) BE733585A (en)
DE (1) DE1927312A1 (en)
FR (1) FR2009680A7 (en)
GB (1) GB1244211A (en)
NL (1) NL6908174A (en)

Also Published As

Publication number Publication date
FR2009680A7 (en) 1970-02-06
NL6908174A (en) 1969-12-02
DE1927312A1 (en) 1970-09-10
BE733585A (en) 1969-11-24

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