GB443242A - Improvements in and relating to the manufacture of azodyestuffs - Google Patents

Improvements in and relating to the manufacture of azodyestuffs

Info

Publication number
GB443242A
GB443242A GB24486/34A GB2448634A GB443242A GB 443242 A GB443242 A GB 443242A GB 24486/34 A GB24486/34 A GB 24486/34A GB 2448634 A GB2448634 A GB 2448634A GB 443242 A GB443242 A GB 443242A
Authority
GB
United Kingdom
Prior art keywords
acid
naphthol
amino
methoxybenzene
nitro
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
GB24486/34A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie 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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Publication of GB443242A publication Critical patent/GB443242A/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
    • C09B43/00Preparation of azo dyes from other azo compounds
    • C09B43/08Preparation of azo dyes from other azo compounds by reduction
    • C09B43/10Preparation of azo dyes from other azo compounds by reduction with formation of a new azo or an azoxy bridge

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
  • Investigating Or Analysing Biological Materials (AREA)

Abstract

Copper complex compounds of azo dyes are made by treating with an agent yielding copper under conditions such that the two alkoxy groups are split up, the dyes obtained by reducing in a caustic alkaline medium with grape sugar a monoazo dyestuff of the general formula <FORM:0443242/IV/1> wherein R1 may be substituted and R2=the residue of the naphthalene or carbazole series containing at least one SO3H group. The products which are probably disazoazoxy dyestuffs yield redder shades on cotton and regenerated cellulose. In examples: (1) the dyestuff 5-nitro-2-amino-1-methoxybenzene --> 1-naphthol-3 : 6-disulphonic acid is reduced and coppered with ammoniacal copper sulphate; 8-chlor-1-naphthol-3 : 6-disulpho acid, 1-naphthol-3 : 8-disulphonic acid and 5-nitro-4-chloro-2-amino-1-methoxybenzene may also be used as components; (2) the dyestuff 5-nitro-2-amino-1-methoxybenzene --> (alkaline) 2-(4<1>-or 3<1>-carboxyphenylamino)-8-naphthol-6-sulphonic acid is treated as above; N-(3<1>-sulphophenyl) 2 : 8 : 6-acid, N-(3<1>-carboxy-phenyl)-J acid or 2-amino-5-naphthol-1 : 7-disulpho acid; (3) and (4) the dyestuffs 5-nitro-2-amino-1-methoxybenzene --> 2-naphthol-5 : 7-, 3 : 6- or 3 : 7-disulpho acid, 1-hydroxycarbazole-3 : 6-disulphonic acid or 1 : 8- or 2 : 8-dihydroxycarbazole - 3 : 6 - disulphonic acid are similarly treated. The Specification as open to inspection under Sect. 91 refers also to the use of functional equivalents of glucose, such as arsenious oxide and formaldehyde as reducing agents and states that the coppering may take place at higher temperatures and under pressure. The ammonia may be replaced by pyridine or other organic base and the reaction may also be performed in acid medium, e.g. with copper sulphate and sodium acetate. This subject-matter does not appear in the Specification as accepted.
GB24486/34A 1933-08-24 1934-08-24 Improvements in and relating to the manufacture of azodyestuffs Expired GB443242A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US443242XA 1933-08-24 1933-08-24

Publications (1)

Publication Number Publication Date
GB443242A true GB443242A (en) 1936-02-24

Family

ID=21931741

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24486/34A Expired GB443242A (en) 1933-08-24 1934-08-24 Improvements in and relating to the manufacture of azodyestuffs

Country Status (1)

Country Link
GB (1) GB443242A (en)

Similar Documents

Publication Publication Date Title
US2427537A (en) Disazo dyes from tetrazotized dihydroxy benzidines
US2203196A (en) Polyazo dyestuffs and process of making same
US2180776A (en) Process for the manufacture of complex metal compounds of polyazo dyestuffs
US1921337A (en) Copper-containing azodyestuff
GB443242A (en) Improvements in and relating to the manufacture of azodyestuffs
US2714588A (en) Copper-containing disazo dyestuffs
US2536957A (en) Process of making metalliferous azo dyestuffs
US2034305A (en) Azo dyestuffs and their production
US2111270A (en) Metalliferous azo dyestuffs and a process for producing same
US2748107A (en) Glucoside azo dyestuffs
GB425990A (en) Process for the manufacture of azodyestuffs containing copper
US2476261A (en) Process for the manufacture of asymmetrical polyazo-dyestuffs
GB561117A (en) Manufacture of metallisable or metallised direct dyestuffs
US2054057A (en) Azo dyestuffs containing chromium
US2712006A (en) Disazo dyestuffs
US2226675A (en) Azo dyestuffs and process of producing same
GB491551A (en) Manufacture of polyazo-dyestuffs
US1885641A (en) Dyestuffs containing metals and process of making same
US2005848A (en) Water insoluble azo dyestuff containing a benzanthrone nucleus
US2047910A (en) Mordant-dyeing monoazo dye and its production
US2557057A (en) Disazo dyestuff
US1819079A (en) Tetrakisazo dye
US2603631A (en) Tetrakisazo dyestuffs
GB744406A (en) Manufacture of azo-dyestuffs
GB571334A (en) Process for the preparation in substance or by metallisation or the like of metal-containing substantive azo dyestuffs