GB383064A - Manufacture of azo-dyestuffs on the fibre - Google Patents

Manufacture of azo-dyestuffs on the fibre

Info

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
Application number
GB31596/31A
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.)
BASF Schweiz AG
Original Assignee
Gesellschaft fuer Chemische Industrie in Basel CIBA
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 Gesellschaft fuer Chemische Industrie in Basel CIBA filed Critical Gesellschaft fuer Chemische Industrie in Basel CIBA
Publication of GB383064A publication Critical patent/GB383064A/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
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/10Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
    • C09B29/18Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides
    • C09B29/20Monoazo 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.
GB31596/31A 1930-11-15 1931-11-14 Manufacture of azo-dyestuffs on the fibre Expired GB383064A (en)

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)

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