GB697480A - Manufacture of monoazo-dyestuffs - Google Patents

Manufacture of monoazo-dyestuffs

Info

Publication number
GB697480A
GB697480A GB164/51A GB16451A GB697480A GB 697480 A GB697480 A GB 697480A GB 164/51 A GB164/51 A GB 164/51A GB 16451 A GB16451 A GB 16451A GB 697480 A GB697480 A GB 697480A
Authority
GB
United Kingdom
Prior art keywords
dimethoxyaniline
benzoylamino
diazotized
oxynaphthoic
dimethylanilide
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
GB164/51A
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.)
C I B A Ltd
Original Assignee
C I B A Ltd
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 C I B A Ltd filed Critical C I B A Ltd
Publication of GB697480A publication Critical patent/GB697480A/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

2 : 3 - Oxynaphthoic - 21 : 61 - dimethylanilide is made by condensing 2 : 3-oxynaphthoic acid or its halide with 2 : 6-dimethylaniline. If the acid is used, a phosphorus halide is added, an example of this method being given. The zinc chloride double salt of the diazonium chloride from 4-benzoylamino-2 : 5-dimethoxyaniline is described and also the diazoamino compound from the latter and N-methyltaurine (sodium salt).ALSO:The invention comprises azo dyes of the formula <FORM:0697480/IV (c)/1> where n is 0 or 1 and the nucleus I may contain non-solubilizing substituents. They are prepared in substance or on the fibre from 2 : 3-oxynaphthoic 21 : 61-dimethylanilide and a diazotized 4-benzoylamino-2 : 5-dimethoxyaniline or 4-phenoxyacetylamino -2 : 5-dimethoxyaniline. When prepared on the fibre, e.g. by printing, the paste may contain the diazo component in a stabilized form and urea may be added. In the examples (1) 4-benzoylamino - 2 : 5 - dimethoxyaniline is diazotized and coupled with 2 : 3 - oxynaphthoic 21 : 61 - dimethylanilide; (2) cotton is grounded with a solution of the arylide in caustic soda and Turkey red oil and developed with diazotized 4 - benzoylamino - 2 : 5 - dimethoxyaniline; (3) cotton is grounded as in (2), dried and printed with the zinc chloride double salt of 4-benzoylamino - 2 : 5 - dimethoxybenzene diazonium chloride together with starch-tragacanth thickener; (4) cotton is printed with a paste of the arylide, the diazoamino compound from diazotized 4 - benzoylamino - 2 : 5 - dimethoxyaniline and N-methyltaurine (sodium salt), Turkey red oil, alcohol, caustic soda and starch-tragacanth thickener; it is then dried, developed by acid steaming, the starch removed by enzymes and the print soaped; the alcohol may be replaced by thiodiglycol and urea added. The following 4 - acylamino - 2 : 5 - dimethoxyanilines are also specified as diazo components:-o-, m- and p - toluylamino, p - tert - butylbenzoylamino, o-, m - and p - chlorobenzoylamino, o -, m - and p - fluorobenzoylamino, o - and p - anisoylamino, o - and p - ethoxybenzoylamino, phenoxyacetylamino and p - tolyloxyacetyl - amino. Specification 303,838, [Class 15 (ii)], and U.S.A. Specification 1,871,946 are referred to.
GB164/51A 1950-01-24 1951-01-02 Manufacture of monoazo-dyestuffs Expired GB697480A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH697480X 1950-01-24

Publications (1)

Publication Number Publication Date
GB697480A true GB697480A (en) 1953-09-23

Family

ID=4529748

Family Applications (1)

Application Number Title Priority Date Filing Date
GB164/51A Expired GB697480A (en) 1950-01-24 1951-01-02 Manufacture of monoazo-dyestuffs

Country Status (1)

Country Link
GB (1) GB697480A (en)

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