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GB1029212A - New azo compounds - Google Patents

New azo compounds

Info

Publication number
GB1029212A
GB1029212A GB803262A GB803262A GB1029212A GB 1029212 A GB1029212 A GB 1029212A GB 803262 A GB803262 A GB 803262A GB 803262 A GB803262 A GB 803262A GB 1029212 A GB1029212 A GB 1029212A
Authority
GB
United Kingdom
Prior art keywords
group
atom
labile
free
acid groups
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
GB803262A
Inventor
John Reginald Atkinson
Eric Hemingway
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 GB803262A priority Critical patent/GB1029212A/en
Publication of GB1029212A publication Critical patent/GB1029212A/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
    • C09B62/00Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/02Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
    • C09B62/022Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring the heterocyclic ring being alternatively specified
    • C09B62/026Azo dyes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

The invention comprises monoazo compounds of the formula <FORM:1029212/C4-C5/1> wherein X stands for any aromatic radical which is free from azo and sulphonic acid groups R1 represents a labile atom or group which is free from sulphonic acid groups, A represents a 1:3:5-triazine or pyrimidine radical and R2 represents a labile atom or group which is free from sulphonic acid groups and which may be the same as or different from that represented by R1 or for a group containing an oxygen, sulphur or nitrogen atom through which it is connected to the triazine or pyrimidine nucleus which is free from sulphonic acid groups and which is not a labile group and the metal complexes of such of these compounds as contain a metallizable group in X in ortho position to the azo group. By a labile atom or group there is meant an atom or group which is free from sulphonic acid groups and which is bound by a covalent bond to a carbon atom of the triazine or pyrimidine nucleus but which readily dissociates under the influence of heat or alkalis, especially in the presence of moisture to form an ion or an uncharged molecule and leave a residue capable of reacting with the cellulose molecule. X may be a benzene, naphthalene or benzthiazole series radical. Such dyes are prepared by reacting appropriate diazonium compounds and coupling components or by reacting a monoazo dye corresponding to the above formula in which at least one of R1 and R2 represents a halogen atom with a tertiary amine or a compound of the formula RH or an alkali metal salt of such a compound where R represents a labile group or a group connected to the hydrogen atom by an O, S or N which is not a labile group. Metal complexes may be prepared by appropriate metallization procedures. In examples: A red dye for polyamides is obtained by diazotizing p-aminoacetanilide and coupling with 2-chloro-4 - di - (b - hydroxyethyl)amino - 6 - (41 -hydroxynaphth - 11 - yl) - 1:3:5 - triazine (1) and a grey dye for wool by chroming the dye 4-nitro-2-aminophenol with [41-chloro-61-di-(b -hydroxyethyl)aminopyrimid - 2 - yl] - 4 - naphthol. Additional examples are furnished.ALSO:4,6 - Dichloro - 2 - (41 - hydroxynaphth - 11 - yl) pyrimidine is obtained by reacting 2: 4: 6-trichloropyrimidine with 1-naphthol in the presence of aluminium chloride and benzene.
GB803262A 1962-03-01 1962-03-01 New azo compounds Expired GB1029212A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB803262A GB1029212A (en) 1962-03-01 1962-03-01 New azo compounds

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB803262A GB1029212A (en) 1962-03-01 1962-03-01 New azo compounds

Publications (1)

Publication Number Publication Date
GB1029212A true GB1029212A (en) 1966-05-11

Family

ID=9844461

Family Applications (1)

Application Number Title Priority Date Filing Date
GB803262A Expired GB1029212A (en) 1962-03-01 1962-03-01 New azo compounds

Country Status (1)

Country Link
GB (1) GB1029212A (en)

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