GB383064A - Manufacture of azo-dyestuffs on the fibre - Google Patents
Manufacture of azo-dyestuffs on the fibreInfo
- Publication number
- GB383064A GB383064A GB31596/31A GB3159631A GB383064A GB 383064 A GB383064 A GB 383064A GB 31596/31 A GB31596/31 A GB 31596/31A GB 3159631 A GB3159631 A GB 3159631A GB 383064 A GB383064 A GB 383064A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chloro
- diphenylether
- amino
- aminodiphenylether
- anisidide
- 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)
- Coloring (AREA)
Abstract
Azo dyes are made on the fibre by coupling an arylide of the general formula <PICT:0383064/IV/1> (in which the benzene nucleus is substituted in at least one of the positions x by an alkyl or alkyloxy group and may be further substituted) with a diazotized 2-amino-1 : 1<1>-diphenylether of the formula NH<2>-R-O-R<1>, in which R may contain, in addition to the NH<2> group, one or more further substituents and R<1> contains at least one substituent, such as halogen, alkyl or alkoxy. Vivid scarlet to blue-red tints are produced fast to light, kier-boiling and chlorine. In examples (1) cotton is impregnated with the o-anisidide or 4-chlor-2-anisidide of 2 : 3-oxynaphthoic acid and developed with diazotized 4 : 4<1>- or 4 : 2<1>-dichloro-2-aminodiphenylether. (2) The material is padded with 2<1> : 3<1>-oxynaphthoyl - 2 - aminohydroquinonedimethylether and printed with a paste containing diazotized 4-chloro-2-amino-4<1>-methyl-1 : 1<1>-diphenylether. In a table the shades produced from the following components are given : diazo components:--4 : 4<1> - dichloroamino diphenylether, 4-chloro-4<1>-methoxy or 4<1>-ethoxy-2 - aminodiphenylether, 4 - chloro - 4<1>-methyl-2-aminodiphenylether; the p-phenetidide, p- and o-toluidide, p-anisidide and 2 : 4-dimethoxyanilide of 2 : 3-oxynaphthoic acid. Specifications 6379/12, [Class 2 (iii), Dyes &c.], 17279/13, 195,600, 202,984 and 310,758, [all in Class 15 (ii), Dyeing, Processes &c. for] are referred to. 2-Amino-1 : 1<1>-diphenylethers above referred to are made by reducing the condensation products from compounds such as 2-nitro-1 : 4-dichlorobenzene, 1-nitro-2 : 4-dichlorobenzene, 1 : 2 - dinitro-5 - chlorobenzene, 2 - nitro - 1 : 4-dibromobenzene and 1 : 2 - dichloro - 4 : 5 - dinitrobenzene with substituted phenols, e.g. o-m, m- or p-cresol, xylenols, o-, m-, or p-chloro-or bromophenol, chlorocresols, dichlorophenols, hydroquinone-monoalkylethers, guaiacol and 1-oxy-3-chloro-6-methoxybenzene. p The Specification as open to inspection under Sect. 91 (3) (a) comprises also the preparation of the above dyestuffs in substance and on a substratum and specifies the dyestuff 4-chloro-2-amino-4<1>-methyl-1 : 1<1>-diphenylether --> 2 : 3-oxynaphthoic acid-o-toluidide. This subject-matter does not appear in the Specification as accepted. Reference has been directed by the Comptroller to Specification 202,984.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH383064X | 1930-11-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB383064A true GB383064A (en) | 1932-11-10 |
Family
ID=4513708
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB31596/31A Expired GB383064A (en) | 1930-11-15 | 1931-11-14 | Manufacture of azo-dyestuffs on the fibre |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB383064A (en) |
-
1931
- 1931-11-14 GB GB31596/31A patent/GB383064A/en not_active Expired
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