GB443242A - Improvements in and relating to the manufacture of azodyestuffs - Google Patents
Improvements in and relating to the manufacture of azodyestuffsInfo
- 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
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
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/08—Preparation of azo dyes from other azo compounds by reduction
- C09B43/10—Preparation 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.
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) |
-
1934
- 1934-08-24 GB GB24486/34A patent/GB443242A/en not_active Expired
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