GB793136A - Improvements in the production of mono- and dis-azo dyestuffs containing chromium - Google Patents

Improvements in the production of mono- and dis-azo dyestuffs containing chromium

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Publication number
GB793136A
GB793136A GB629356A GB629356A GB793136A GB 793136 A GB793136 A GB 793136A GB 629356 A GB629356 A GB 629356A GB 629356 A GB629356 A GB 629356A GB 793136 A GB793136 A GB 793136A
Authority
GB
United Kingdom
Prior art keywords
amino
methyl
naphthol
sulphonamide
methoxy
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
GB629356A
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 SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik 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 BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Priority to GB629356A priority Critical patent/GB793136A/en
Publication of GB793136A publication Critical patent/GB793136A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Chromium - containing o : o1 - dihydroxy - azo dyestuffs which contain two identical or different dyestuff molecules for each chromium atom are prepared by treating an o-alkoxy-o1-hydroxy-azo dyestuff or a mixture of two or more dyestuffs of the said kind at an elevated temperature and in the presence of an organic solvent, with compounds of hexavalent chromium and with reduction of the chromium compounds. A solvent having a reducing action on the chromium compounds is preferably used. Specified solvents are mono- and polyhydric alcohols and their esters and ethers, dioxan tetrahydrofuran, butyrolactone, ethanolamine and carboxylic acid amides. Substances which may be used to reduce the chromium compounds are salts and esters of sulphurous, thiosulphuric or arsenious acids and mono- and di-saccharides. Specified compounds of bevalent chromium are alkali metal mono- and dichromates. In an example the dyestuff 1-amino - 2 - methoxy - 5 - methyl - benzene - 4 - sulphonamide --> 1 - phenyl - 3 - methyl - 5 - pyrazolone is mixed with b : b 1-dihydroxyethyl ether and sodium chromate, heated, diluted with water and the chromium complex salted out. Azo dyestuffs prepared from the following components are treated in a similar manner to give their chromium complexes: diazo components: 1 - amino - 2 - methoxybenzene, 1 - amino - 2 - methoxy - 5 - chloro - or - methyl - benzene, 1 - amino - 2 - methoxy - 4 - or - 5 - nitrobenzene, 1 - amino - 2 - methoxy - 4 - nitro - 5 - chloro - benzene, 1 - amino - 2:4 - or - 2:5 - dimethoxybenzene, 1 - amino - 2:5 - diethoxybenzene, 1 - amino - 2 - methoxy - 4 - chloro - 5 - methylbenzene, 1-amino-2:4- or -2:5-dimethoxy - 4 - chlorobenzene, 1 - amino - 2 - methoxy - 4 - phenylamino - benzene, 1 - amino - 2 - methoxybenzene - 5 - carbonamide or -sulphonamide or -sulphomethylamide or -sulphophenylamide or -sulphodiethylamide or -sulpho-(31- or 41-sulphonamido-phenyl)-amide or -methyl or -benzyl sulphone, 1-amino-2-methoxy-5-methylbenzene-4-sulphonamide or -sulphomethylamide or -sulphophenylamide or -sulpho-N-ethyl-N-(21-hydroxy)-ethyl-amide or -methyl sulphone, 1 - amino - 2 - methoxy - 5 - chlorobenzene - 4 - ethylsulphone or-sulphonamide or -sulphomethylamide or -sulphophenylamide, 1-amino-2:5 - dimethoxy - 4 - benzoylaminobenzene, 1 - amino - 2:5 - diethoxy - 4 - acetylaminobenzene, 1 - amino - 2:5 - dimethoxybenzene - 4 - sulphonamide or -sulphomethylamide or -methyl sulphone, 1-amino-2:5-diethoxybenzene - 4 - sulphonamide or -sulphophenylamide, 1 - amino - 2 - ethoxy - naphthalene, 1 - amino - 2 - methoxy - 4 - (41 - sulphonamido - phenylazo) - 5 - methylbenzene and 1 - amino - 2:5 - dimethoxy - 4 - (31 - sulphonamido - phenylazo)-benzene; coupling components:-4 -methyl- or -acetylamino- or -isobutylphenol, 2:4-dichlorophenol, 2-naphthol, 2-naphthol-6-sulphonamide or -sulphophenylamide or -sulpho-N-(21-hydroxy)-ethylamide or -sulphodimethylamide or -sulpho-N-methyl-N-(21-hydroxy)-ethylamide, 2-naphthol-4-sulphonamide or -sulphomethylamide or -sulphophenylamide, 2-naphthol-7-sulphonamide, 2-naphthol-5-sulphomethylamide, 1-naphthol-3- or -4-sulphonamide, 1-naphthol-3:6-disulphonamide or -disulphomethylamide, 2-naphthol-3:6-disulphonamide, 6-bromo-2-naphthol, 5:8-dichloro-1-naphthol, 8-acetylamino- or -carbomethoxyamino-2-naphthol, 1-phenyl- or -(21-methylphenyl)- or -(31- or 41-sulphamidophenyl)- or -(41-methyl-31-sulphamidophenyl)- or -(31- or 41-methylsulphonylphenyl)- or -(21-chloro-51-sulphonamidophenyl)-or -(21:51-dichlorophenyl)- or -(31-chloro- or - nitro - phenyl) - or - (41 - benzenesulphaminophenyl) - 3 - methyl - 5 - pyrazolone, 1 - phenyl - 3-carboethoxy- or -carbonamido-5-pyrazolone, 3 - methyl - 5 - pyrazolone, 1:3 - diphenyl - 5 - pyrazolone, 2:4 - dihydroxyquinoline and 1 - methyl - 4 - hydroxy - quinolone (2). Specification 758,016 is referred to.
GB629356A 1956-02-29 1956-02-29 Improvements in the production of mono- and dis-azo dyestuffs containing chromium Expired GB793136A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB629356A GB793136A (en) 1956-02-29 1956-02-29 Improvements in the production of mono- and dis-azo dyestuffs containing chromium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB629356A GB793136A (en) 1956-02-29 1956-02-29 Improvements in the production of mono- and dis-azo dyestuffs containing chromium

Publications (1)

Publication Number Publication Date
GB793136A true GB793136A (en) 1958-04-09

Family

ID=6708849

Family Applications (1)

Application Number Title Priority Date Filing Date
GB629356A Expired GB793136A (en) 1956-02-29 1956-02-29 Improvements in the production of mono- and dis-azo dyestuffs containing chromium

Country Status (1)

Country Link
GB (1) GB793136A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3051696A (en) * 1960-03-23 1962-08-28 Du Pont Chromation of azo dyes

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3051696A (en) * 1960-03-23 1962-08-28 Du Pont Chromation of azo dyes

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