GB476493A - Improvements in the manufacture and production of azo dyestuffs - Google Patents
Improvements in the manufacture and production of azo dyestuffsInfo
- Publication number
- GB476493A GB476493A GB1588136A GB1588136A GB476493A GB 476493 A GB476493 A GB 476493A GB 1588136 A GB1588136 A GB 1588136A GB 1588136 A GB1588136 A GB 1588136A GB 476493 A GB476493 A GB 476493A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- azaphenanthrene
- amides
- acid
- aminobenzene
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/18—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides
- C09B29/20—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides of the naphthalene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Azo dyes are made in substance or on the fibre by coupling o-hydroxycarboxylic acid amides in which one hydrogen atom of the amide group is replaced by the radicle of a mono-azaphenanthrene with diazo compounds of cyclic amines. Since the amides are in some cases soluble in acid the treatment on the fibre may be carried out in acid solution. In examples (1)-(3) the following dyes are formed on cotton according to the usual method, (1) and (2) 1-omega-trifluoromethyl-3-aminophenyl-4-ethylsulphone --> 2<1>.3<1>-hydroxynaphthoyl - 9 - or 10 - amino - 4-azaphenanthrene (scarlet-red); other diazo components specified are 4-chloro-3-aminobenzotrifluoride, o- or p-nitroaniline, 2 : 5-dichloraniline, 1-amino-2-methoxy-5-ethyl- or benzylsulphonebenzene, 1-methyl-2-amino-5-chlor- or 5-nitrobenzene, 1-amino-3-methyl-4-nitrilo-6-chlorobenzene, m-chloraniline, 2-aminodiphenyl sulphone 1-methyl-3-nitro-4-aminobenzene; the corresponding amides from o-hydroxycarboxyazanaphthalenes and o-hydroxycarboxyazaphenanthrenes may also be used; (3) 1-amino-3-methyl-4-cyano-6-chlorobenzene --> 2<1> : 3<1>-hydroxynaphthoyl-8-amino-4-azaphenanthrene (brick red); additional diazo components specified are 1-amino-2-trifluormethyl-4-chlorbenzene, 4-amino-4<1>-methoxydiphenylamine, 4-aminodiphenylamine, 1-methoxy-2-amino-5-nitrobenzene, 1-methoxy-3-nitro-4-aminobenzene; 4-benzoylamino-2 : 5-diethoxy-1 - aminobenzene or 4 - amino - 3 - methoxydiphenylamine --> 2<1> : 3<1>-hydroxyanthracenoyl-9- or 10-amino-4-azaphenanthrene; 4-benzoylamino - 2 : 5 - dimethoxy - 1 - aminobenzene, dianisidine, 4-amino-4<1>-methoxydiphenylamine or 3 - amino - 4 - methoxy - 6 - benzoylamino - 1-methylbenzene --> 2<1> : 3<1> - hydroxyanthracenoyl - 10 - amino - 4 - azaphenanthrene; the amides from benzofurane-o-hydroxycarboxylic acids or o-hydroxyphenanthrene carboxylic acids and aminoazaphenanthrenes are also specified; (4) a mixed fabric of staple fibre (Zellwolle) and wool is impregnated with a solution containing 2<1> : 3<1>-hydroxynaphthoyl-10-amino-4-azaphenanthrene, ammonia, ethanol and a dispersing agent and developed with diazotized o-phenetidine --> a -naphthylamine (black); additional components include o-chloraniline, 2 - chlor - 4 - nitroaniline, 6 - chlor-2-toluidine, 4 : 4<1> - dichlor - 2 - aminodiphenylether, 4-amino-2 : 5-dimethoxy-2<1> : 6<1>-dichlor-4<1>-nitroazobenzene and 4-aminodiphenylamine. Other arylides specified are those from 2 : 3-oxynaphthoic acid and monoamino-2- or 3-azaphenanthrenes. Those derived from other carboxylic acids, e.g. 2 : 3-hydroxycarbazolecarboxylic acid, 2 : 3-hydroxydiphenylene carboxylic acids or from 2 : 3-hydroxycarboxylic acids of azaphenanthrenes, azanaphthalenes, anthracene or phenanthrene may also be used as well as those from 2 : 3-oxynaphthoic acid and diaminoazaphenanthrenes and substituted aminoazaphenanthrenes. Specification 463,456 is referred to. The amides from o-hydroxyazanaphthalene and o-hydroxyazaphenanthrene carboxylic acids (obtained by action of carbon dioxide on the alkali salts of hydroxyazanaphthalenes and hydroxyazaphenanthrenes) are made by converting the acids into their acetoxy derivatives by means of acetic anhydride, reacting with thionyl chloride to form the corresponding chlorides, condensing the latter with aminoazaphenanthrenes and splitting off the acetyl group.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1588136A GB476493A (en) | 1936-06-06 | 1936-06-06 | Improvements in the manufacture and production of azo dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1588136A GB476493A (en) | 1936-06-06 | 1936-06-06 | Improvements in the manufacture and production of azo dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB476493A true GB476493A (en) | 1937-12-06 |
Family
ID=10067207
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1588136A Expired GB476493A (en) | 1936-06-06 | 1936-06-06 | Improvements in the manufacture and production of azo dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB476493A (en) |
-
1936
- 1936-06-06 GB GB1588136A patent/GB476493A/en not_active Expired
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