GB417258A - New dyestuff intermediates and azo dyes therefrom - Google Patents
New dyestuff intermediates and azo dyes therefromInfo
- Publication number
- GB417258A GB417258A GB883433A GB883433A GB417258A GB 417258 A GB417258 A GB 417258A GB 883433 A GB883433 A GB 883433A GB 883433 A GB883433 A GB 883433A GB 417258 A GB417258 A GB 417258A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chromium
- coupled
- amino
- diazotized
- acid
- 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Chromium compounds of amino-o-hydroxycarboxydiarylsulphones are made by treating at raised temperature an aminodiarylsulphone, carrying in o-position to one another a hydroxyl and a carboxyl group, with a chromium-providing compound, e.g. aqueous chromium fluoride. The sulphones produced by the processes of Specifications 245,865, 297,855, [both in Class 2 (iii)], and 417,252 may be used. In examples, (1) 2-amino-3<1>-hydroxy-4<1>-carboxydiphenylsulphone-4 -sulphonic acid is treated with the ennea hydrate of chromium fluoride. Azo dyes containing chromium are made by diazotizing the chromium compounds of the above aminodiarylsulphones and coupling with components. In further examples, (2)--(4) the chromium compound of 2 - amino - 3<1> - hydroxy - 4<1> - carboxydiphenylsulphone - 4 - sulphonic acid is diazotized and coupled with 1 -(2 : 5-dichloro-4-sulphophenyl)-3-methyl-5-pyrazolone (greenish yellow), b - naphthol (orange), 2 : 8 : 6-acid (bluish-red), H acid (coupled with 2 mols. of the diazo compound) (grey to reddish-grey); (5) the same chromium compound is diazotized and coupled with m-amino-p-cresol methylether, again diazotized and coupled with phenyl-J acid (red-violet). If the chromium-free aminosulphones are diazotized and coupled insoluble products are obtained on chroming.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB883433A GB417258A (en) | 1933-03-23 | 1933-03-23 | New dyestuff intermediates and azo dyes therefrom |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB883433A GB417258A (en) | 1933-03-23 | 1933-03-23 | New dyestuff intermediates and azo dyes therefrom |
Publications (1)
Publication Number | Publication Date |
---|---|
GB417258A true GB417258A (en) | 1934-09-24 |
Family
ID=9860095
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB883433A Expired GB417258A (en) | 1933-03-23 | 1933-03-23 | New dyestuff intermediates and azo dyes therefrom |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB417258A (en) |
-
1933
- 1933-03-23 GB GB883433A patent/GB417258A/en not_active Expired
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