GB358483A - Process for the manufacture of azo dyestuffs - Google Patents

Process for the manufacture of azo dyestuffs

Info

Publication number
GB358483A
GB358483A GB2023930A GB2023930A GB358483A GB 358483 A GB358483 A GB 358483A GB 2023930 A GB2023930 A GB 2023930A GB 2023930 A GB2023930 A GB 2023930A GB 358483 A GB358483 A GB 358483A
Authority
GB
United Kingdom
Prior art keywords
naphthol
acid
aminobenzene
sulphonic acid
fulling
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
GB2023930A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie 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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB2023930A priority Critical patent/GB358483A/en
Publication of GB358483A publication Critical patent/GB358483A/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
    • C09B29/16Naphthol-sulfonic acids

Landscapes

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

Abstract

Monoazo dyes are obtained by coupling a sulphonated aromatic diazo compound, other than an o-oxydiazo compound, with a 1-naphthol-3 : 6-disulphonamide or an N-substituted derivative or an 8-halogen derivative thereof or with a 1-naphthol-3 : 7-disulphonamide or an N-substituted derivative thereof. The products yield clear even dyeings, fast to light, washing, and fulling, on wool and are suitable for the manufacture of lakes and for printing. The following examples are specified (1) The dyestuff, aniline - 2-sulphonic acid -->-1-naphthol-3 : 6-disulphonic acid-di-(N-methyl-anilide), dyes wool a clear even orange fast to fulling and light; the corresponding products having as diazo components 4-methyl-1-aminobenzene-2-sulphonic acid 4-methoxy 1-aminobenzene-2-sulphonic acid, and 4-acetylamino-1-aminobenzene-2-sulphonic acid dye wool similar blueish red shades. (2) The dyestuff, 4-methyl-1-aminobenzene-2-sulphonic acid --> 1-naphthol-3 : 6-disulphonic acid-dianilide, dyes wool an even yellowish red, fast to fulling and light; similar dyestuffs are obtained with the use as diazo components of other aminosulphonic acids of the benzene series containing no o-oxyamino group and with the use as coupling components of the corresponding chloranilides and toluidides. (3) The dyestuff, 4-chloro-1-aminobenzene-2-sulphonic acid --> 1-naphthol-3 : 6-disulphonic acid di-(N-b -hydroxyethyl-anilide), dyes wool a very even yellowish red fast to light and fulling; similar dyestuffs are obtained with the use as diazo components of other aminosulphonic acids of the benzene series containing no o-oxyamino group, e.g. 4-methyl-1-aminobenzene-2-sulphonic acid and 4-acetylaminobenzene-2-sulphonic acid. (4) The dyestuff, 4-methyl-1 - aminobenzene - 2 - sulphonic acid- --> 1-naphthol-3 : 6-disulphonic acid-di-(31-acetylaminoanilide), dyes wool a clear, very even, yellowish red, very fast to light and fulling; similar dyestuffs are obtained with the use as diazo components of other aminosulphonic acids of the benzene series containing no o-oxyamino-group and with the use as coupling component of 1-naphthol-3 : 6-disulphonic acid-di- (41-acetylaminoanilide). (5) The dyestuff, 4-methyl - 1 - aminobenzene- 2- sulphonic acid --> 8-chloro-1-naphthol-3 :6-disulphonic acid-dianilide, dyes wool a very even clear red, fast to fulling and light. (6) The dyestuffs, 1-amino-2-ethoxynaphthalene-6 - sulphonic acid --> 1 - naphthol-3 : 6-disulphonic acid-di- (31 [or 41]-acetylaminoanilide), dye wool very even clear violet shades fast to washing and fulling. (7) The dyestuff, 4-acetylamino-1 - aminobenzene - 2-sulphonic acid --> 1-naphthol-3 : 7-disulphonic acid-dianilide dyes wool an even blueish red fast to fulling, washing, and light. 1-Naphthol-3 : 6 (or 3 : 7)-disulphonamides and their N-substituted derivatives are obtained by heating the 1-naphthol-3 : 6 (or 3 : 7)-disulphochlorides with ammonia or the corresponding amines in presence of an acid-binding agent, e.g. sodium acetate. 8-chloro-1-naphthol-3 : 6-disulphonic acid-dianilide is obtained according to the process described in Specification 232,620, [Class 2 (iii), Dyes &c.].
GB2023930A 1930-07-03 1930-07-03 Process for the manufacture of azo dyestuffs Expired GB358483A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2023930A GB358483A (en) 1930-07-03 1930-07-03 Process for the manufacture of azo dyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2023930A GB358483A (en) 1930-07-03 1930-07-03 Process for the manufacture of azo dyestuffs

Publications (1)

Publication Number Publication Date
GB358483A true GB358483A (en) 1931-10-05

Family

ID=10142685

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2023930A Expired GB358483A (en) 1930-07-03 1930-07-03 Process for the manufacture of azo dyestuffs

Country Status (1)

Country Link
GB (1) GB358483A (en)

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