GB759353A - Manufacture of water-insoluble azo-dyestuffs from 2:3-hydroxynaphthoic acid arylides - Google Patents

Manufacture of water-insoluble azo-dyestuffs from 2:3-hydroxynaphthoic acid arylides

Info

Publication number
GB759353A
GB759353A GB13319/52A GB1331952A GB759353A GB 759353 A GB759353 A GB 759353A GB 13319/52 A GB13319/52 A GB 13319/52A GB 1331952 A GB1331952 A GB 1331952A GB 759353 A GB759353 A GB 759353A
Authority
GB
United Kingdom
Prior art keywords
azo
amino
nitro
chloro
benzene
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
GB13319/52A
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.)
Hoechst AG
Original Assignee
Hoechst AG
Farbwerke Hoechst AG
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 Hoechst AG, Farbwerke Hoechst AG filed Critical Hoechst AG
Publication of GB759353A publication Critical patent/GB759353A/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
    • C09B33/00Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
    • C09B33/02Disazo dyes

Landscapes

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

Abstract

The invention comprises water-insoluble dyestuffs of formula <FORM:0759353/IV(c)/1> where R and R1 are aromatic radicles free of groups imparting solubility in water and X is an alkyl or esterified carboxyl group. They are made by coupling in substance, on the fibre or on a substratum suitable for producing lakes on appropriate 2, 3-hydroxynaphthoic acid arylide with a diazo- or diazo-azo-compound free of groups imparting solubility in water other than the diazo group. Preferred diazo-azo-compounds are those of formula <FORM:0759353/IV(c)/2> where A and B may be substituted and especially those where B contains a sulphonic acid group. The arylides are made by condensing 2, 3-hydroxynaphthoic acid or a functional derivative thereof with an appropriate amino-azo-dyestuff. The arylides are novel and dye vegetable fibres in reddish to greenish yellow tints. The amino-azo-dyestuffs are made by coupling an appropriate aminophenyl-pyrazolone with a diazotized amine in a neutral to feebly alkaline medium. When produced in substance the dis-azo dyestuffs yield pigments. Advantageously they are produced on the fibre by processes used in the production of ice colours. The preparation of certain of the monoazo starting arylides is described in detail and examples and tables are provided of the preparation of the dyestuffs and their use in dyeing processes the arylides used and/or prepared being derived from 2, 3-hydroxynaphthoic acid or functional derivatives thereof and the following pyrazolones: - 1 - 31 - aminophenyl) - 3 - methyl - 4 - (11 - methoxy - 411 - and - 511 - chloro - , 211 - metyl - 411 - chloro - and 211 - trifluoromethyl - 411 - chloro - benzene - 111 - azo) -, (311 - chlorobenzene - 111 - azo) - and - (naphthalene - 111 - azo) -, 1 - (31 - aminophenyl) - 3 - carboethoxy - 4 - (211 - methyl - 411 - chloro - benzene - 111 - azo) - and 1 - (41 - aminophenyl) - 3 - methyl - 4 - (311 - chloro - and 211 - methyl - 411 - chloro-benzene - 111 - azo) - 5 - pyrazolone the diazo - and diazo - azo - components with which they are coupled being 1 - amino - 4 - (21 - methoxy - 51 - nitro - and 21,41 - dimethoxy-51 - nitro - benzene - 11 - azo) - 2 - ethoxy - naphthalene, 1 - amino - 4 - (21 - methyl-51 - nitro - and 21 - chloro - 51 - nitro - benzene - 11 - azo) - 2 ethoxynaphthalene - 6 - sulphonic acid, 1 - amino - 4 - (21 - methyl - 51 - nitro - benzene - 11 - azo) - 7-methoxynaphthalene, 1 - amino - 4 - (21, 51 - dichloro - and 21 - methoxy - 51 nitro - benzene - 11 - azo) - 2 - methoxynaphthalene-6-sulphonic acid, 1 - amino - 2 - (41 - nitro - 21 - chlorobenzene - 11 - azo) - 3 - methoxy - 4 - methylbenzene, 1 - amino - 4 - (41 - nitro-benzene - 11 - azo) - 2, 5 - diamethoxybenzene, p-nitraniline, 1 - amino - 2,5 - dichlorobenzene, 1 - aminoanthraquinone, 4 - aminodiphenylamine, 4 - amino - 3 - methoxydiphenylamine, 1 - amino - 2 - methoxy - 4 - benzoylamino - 5 - methylbenzene, 1 - amino-4-chloro - 2 - methylbenzene, 1 - amino - 4 - nitro - 2 - methoxybenzene and 1 - amino - 4 - benzoylamino - 2, 5 - diethoxybenzene. In the examples cotton is dyed in red, brown, green, black, blue and orange shades. Specification 367,907 is referred to.
GB13319/52A 1951-05-26 1952-05-26 Manufacture of water-insoluble azo-dyestuffs from 2:3-hydroxynaphthoic acid arylides Expired GB759353A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE759353X 1951-05-26

Publications (1)

Publication Number Publication Date
GB759353A true GB759353A (en) 1956-10-17

Family

ID=6660492

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13319/52A Expired GB759353A (en) 1951-05-26 1952-05-26 Manufacture of water-insoluble azo-dyestuffs from 2:3-hydroxynaphthoic acid arylides

Country Status (1)

Country Link
GB (1) GB759353A (en)

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