GB515099A - Manufacture of new dyestuffs - Google Patents

Manufacture of new dyestuffs

Info

Publication number
GB515099A
GB515099A GB15310/38A GB1531038A GB515099A GB 515099 A GB515099 A GB 515099A GB 15310/38 A GB15310/38 A GB 15310/38A GB 1531038 A GB1531038 A GB 1531038A GB 515099 A GB515099 A GB 515099A
Authority
GB
United Kingdom
Prior art keywords
acid
amino
group
pyrazolone
dehydrothiotoluidine
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
GB15310/38A
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 GB515099A publication Critical patent/GB515099A/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
    • C09B45/00Complex metal compounds of azo dyes
    • C09B45/02Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
    • C09B45/14Monoazo compounds

Landscapes

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

Abstract

515,099. Dyes. SOC. OF CHEMICAL INDUSTRY IN BASLE. May 23, 1938, Nos. 15310 and 15311. Convention dates, May 22, 1937, and April 27, 1938. [Classes 2 (iii) and 15 (ii)] Azo dyes are made by combining a compound of the general formula in which R1 is a benzene nucleus to which the group -NHX- is linked in a' position other than an o-position to the arylthiazole residue, R2 is the residue of a 1-phenyl-5-pyrazolone linked to X in 4<1>-or 31-position of the phenyl residue and X = -CONH- or -(triazine residue)-NH-, with a diazo compound substituted in o-position to the diazo group by a COOH group or by a group which can be converted into a COOH group, and converting the product so obtained into a complex metal compound in substance or on the fibre, the said 'group in o-position to the diazo group (if it is not a COOH group) being converted into a COOH group before or simultaneously with the metallization. They yield yellow to orange and brown shades on cellulose or regenerated cellulose. In the examples (1) the urea from dehydrothiotoluidine-mono-sulphonic acid and 1-(3<1>- or 41-aminophenyl)-5- pyrazolone-3-carboxylic acid is coupled with diazotized 1-amino-4-sulphobenzene-2-carboxylic acid or anthranilic acid and the dyestuff treated with ammoniacal copper sulphate ; the coupling component may also be the tertiary condensation product from cyanuric chloride and 1-(4<1>- or 31-aminophenyl)-3- methyl- or 3-carboxy-5-pyrazolone, dehydrothiotoluidine monosulphonic acid and aniline, (2)-(4) examples of dyeing processes. Other components specified are the condensation products from 3<1>- or 4<1>-aminoaryl-5-pyrazolones and Á-aminophenylarylthiazoles ; 1- aminobenzene-4-nitro-2-carboxylic acid, anthranilic acid ethyl ester. Specification 299,331, [Class 2 (iii)], is referred to. The Specification as open to inspection under Sect. 91 comprises the manufacture of azo dyes by combining a Á-phenylarylthiazole in which the Á-phenyl nucleus is linked to a 5-pyrazolone nucleus with a diazo compound substituted in o-position to the diazo group by a group which in combination with the enolizable CO-group of the pyrazolone is capable of yielding complex metal compounds, or by a substituent which can be converted into such a group, and converting the product so obtained into a complex metal compound. Additional components specified are 1-amino- 4-chlor-2-phenol, 1-amino-4-nitro-2-phenol, 1-amino-2-phenol-4-sulphonic acid or 4:6- disulphonic acid, 1-amino-2-chlorbenzene-4- sulphonc acid, 1-amino-2-methoxybenzene- 4-sulphonic acid, 1-amino-2-naphthol-4- sulphonic acid, 2-amino-1-naphthol-4: 8- disulphonic acid ; the condensation products from acetoacetic esters or oxalacetic esters and the hydrazine from dehydrothiotoluidine, the condensation 'products from 1-phenyl-3- methyl-5-pyrazolone-31- or 41-carboxylic acid and dehydrothiotoluidine or dehydrothioxylidine and sulphonic acids of such compounds, compounds resulting from the combination of amino-5-pyrazolones and Á-aminophenylarylthiazoles by means of compounds containing at least two reactive halogen atoms. In examples (1) 1-phenyl-3-methyl-5-pyrazole-4<1>-carboxylic acid is condensed with dehydrothiotoluidinemonosul-phonic acid by means of pyridine, dimethyl-aniline and phosphorus trichloride, the product coupled with diazotized 1-amino-4-sulpho-benzene-2-carboxylic acid and the dyestuff treated with' ammoniacal copper sulphate ; the coupling component may also be made by condensing p-nitrobenzoyl chloride with dehydrothiotoluidine monosulphonic acid, reducing, diazotizing, converting to the hydrazine and condensing with ethylacetoacetate, (2) similar to (1) using dehydrothiotoluidine instead of the sulphonic acid and chlorbenzene instead of pyridine and dimethylaniline ; the copper compound may also be produced on the fibre, (3) diazotized dehydrothiotoluidine is reduced with stannous chloride, the hydrazine obtained condensed with ethyl acetoacetate to form the pyrazolone which is coupled with diazotized 1-amino-4-sulphobenzene-2- carboxylic acid or 2-aminophenol sulphonic acid and the dyestuff coppered in substance or on the fibre, (4) 6-sulpho-1 : 2-naphtho-Á- (3<1>-amino)-phenylthiazole is condensed with p-nitrobenzoyl chloride, the product reduced with NaHS, diazotized, reduced to the hydrazine, condensed with ethyl acetoacetate and the pyrazolone obtained coupled with diazotized 2-amino-4-sulphobenzene-l-carboxylic acid and the dyestuff coppered ; anthranilic acid or an o-aminophenol or a sulphonic acid thereof may also be used. This subject-matter does not appear in the Specification 'as accepted.
GB15310/38A 1937-05-22 1938-05-23 Manufacture of new dyestuffs Expired GB515099A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH515099X 1937-05-22

Publications (1)

Publication Number Publication Date
GB515099A true GB515099A (en) 1939-11-27

Family

ID=4517651

Family Applications (1)

Application Number Title Priority Date Filing Date
GB15310/38A Expired GB515099A (en) 1937-05-22 1938-05-23 Manufacture of new dyestuffs

Country Status (1)

Country Link
GB (1) GB515099A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2153835A (en) * 1984-02-10 1985-08-29 Sandoz Ltd Triazinyl azo dyestuffs and intermediates

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2153835A (en) * 1984-02-10 1985-08-29 Sandoz Ltd Triazinyl azo dyestuffs and intermediates

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