GB578964A - Manufacture of disazo-and polyazo-dyestuffs - Google Patents

Manufacture of disazo-and polyazo-dyestuffs

Info

Publication number
GB578964A
GB578964A GB13913/43A GB1391343A GB578964A GB 578964 A GB578964 A GB 578964A GB 13913/43 A GB13913/43 A GB 13913/43A GB 1391343 A GB1391343 A GB 1391343A GB 578964 A GB578964 A GB 578964A
Authority
GB
United Kingdom
Prior art keywords
oxy
pyrazolone
methyl
dyes
carboxyphenyl
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
GB13913/43A
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 GB578964A publication Critical patent/GB578964A/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
    • C09B35/00Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

Azo dyes; dyeing regenerated cellulose.-Dis- or poly-azo dyes are made by coupling any components with a 3-oxy-31-alkoxy-4 : 41-diaminodiphenyl, and, if desired, performing a further coupling or linking reaction or reactions. Coupling components may be benzene, naphthalene or heterocyclic derivatives and may contain the carbon atom capable of coupling in an open chain, the following being specified: phenols, salicylic acid, resorcinol, naphthols, naphthol mono- or di-sulphonic acids, aminonaphthols and sulphonic acids thereof, 1-aryl-3-methyl- or carboxy-pyrazolones with or without substituents such as sulphonamido, nitro, amino or salicylic acid groups in the aryl nucleus, and acetoacetic arylides. Especially valuable dyes are obtained by using a pyrazolone as one component and/or a component containing the salicylic acid grouping. These two features may be present together, e.g. by using 1-(31-carboxy-41-oxyphenyl)-3-methyl-5-pyrazolone. Tris- and poly-azo dyes are made by using components (a) containing a further diazotisable amino group or a group capable of conversion thereto, (b) capable of coupling more than once or (c) suitable for producing polyazo dyes by other reactions, e.g. by formation of ureas or reduction of two nitro-groups. The dyes are suitable for dyeing or printing animal fibres, e.g. wool, silk and leather and cellulosic fibres, e.g. cotton, linen, artificial silk and staple fibre of regenerated cellulose. The dyes may be reacted with agents yielding metal, especially copper, e.g. complex copper tartrates, in substance, in the dyebath or on the fibre. In examples (1) to (8), disazo dyes are prepared from 3-oxy-31-methoxybenzidine and the following: salicylic acid and 1-(31-sulphonamidophenyl) - 3 - methyl - 5 - pyrazolone, the latter component alone, salicylic acid and 1-(41-oxy-31 - carboxyphenyl) - or 1 - (31 - nitrophenyl)- or 1 - (41-b -oxyethoxyphenyl)-3-methyl-5-pyrazolone or 3 - methyl - 5 - pyrazolone, 1 - amino - 8 - naphthol - 4 - sulphonic acid, 5 : 51 - dioxy - 2 : 21-dinaphthylamine - 7 : 71 - disulphonic acid and 1 - (41 - oxy - 31 - carboxyphenyl) - 3 - methyl - 5 - pyrazolone; polyazo dyes from 3-oxy-31-methoxybenzidine and the following: salicylic or o- or m-cresotinic acid and 1-(31- or 41-aminophenyl)-3-methyl-5-pyrazolone --> 1-(41-oxy-31 - carboxyphenyl)- or 1 - (41 - b - oxyethoxyphenyl) - 3 - methyl - 5 - pyrazolone, 2 - amino- or 2 - (41 - oxy - 31 - carboxyphenyl) - amino - 5 - oxynaphthalene - 7 - sulphonic acid or 2 - aminophenol - 4 - sulphonamide --> resorcinol, and 2-aminophenol-4-sulphonamide or 4-nitro-2-aminophenol --> resorcinol and 1-(41-oxy-31-carboxyphenyl) - 3 - methyl - 5 - pyrazolone. In example (9) cotton is dyed with salicylic acid \sM 3 - oxy - 31 - methoxybenzidine --> 1 - (41-oxy-31-carboxyphenyl)-3-methyl-5-pyrazolone and treated with complex copper tartrate in the dyebath. Specification 455,274 is referred to. 3-Oxy-31-methoxybenzidine is made by the partial saponification of dianisidine with moderately concentrated (e.g. 65 per cent) sulphuric acid. The crude product, containing some 3.31-dioxybenzidine, may be extracted with chlorobenzene and the extracted 3-oxy-31-methoxybenzidine purified by recrystallisation from benzene.
GB13913/43A 1942-09-02 1943-08-26 Manufacture of disazo-and polyazo-dyestuffs Expired GB578964A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH578964X 1942-09-02

Publications (1)

Publication Number Publication Date
GB578964A true GB578964A (en) 1946-07-18

Family

ID=4521381

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13913/43A Expired GB578964A (en) 1942-09-02 1943-08-26 Manufacture of disazo-and polyazo-dyestuffs

Country Status (1)

Country Link
GB (1) GB578964A (en)

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