GB414684A - Process for the manufacture of azodyestuffs and intermediate products therefor - Google Patents

Process for the manufacture of azodyestuffs and intermediate products therefor

Info

Publication number
GB414684A
GB414684A GB3904/33A GB390433A GB414684A GB 414684 A GB414684 A GB 414684A GB 3904/33 A GB3904/33 A GB 3904/33A GB 390433 A GB390433 A GB 390433A GB 414684 A GB414684 A GB 414684A
Authority
GB
United Kingdom
Prior art keywords
pyrazolone
dehydrothiotoluidine
pyrazolones
aniline
fibre
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
GB3904/33A
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
Publication of GB414684A publication Critical patent/GB414684A/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
    • C09B29/34Monoazo dyes prepared by diazotising and coupling from other coupling components
    • C09B29/36Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
    • C09B29/3604Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
    • C09B29/3647Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms
    • C09B29/3652Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms containing a 1,2-diazoles or hydrogenated 1,2-diazoles
    • C09B29/366Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms containing a 1,2-diazoles or hydrogenated 1,2-diazoles containing hydroxy-1,2-diazoles, e.g. pyrazolone

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Coloring (AREA)

Abstract

Water-insoluble azo dyes are made in substance, on the fibre or on a substratum, by coupling a diazo or tetrazo compound with one or two molecular proportions respectively of a pyrazolone derived from an aminoarylthiazole. The following dyestuffs are described in examples: 2-nitraniline --> the 3-methyl-5-pyrazolone from dehydrothiotoluidine (in substance) and on the fibre using the following diazo components: 5-chlor-2-methyl-1-aniline, 2-aminoanthraquinone, 4-amino-3 : 2<1>-dimethylazobenzene and 4-benzoylamino-2 : 5-dimethoxy-1-aniline. Yellow to red shades fast to washing and light are obtained. The pyrazolones from dehydrothioxylidine and primuline are also specified. Samples have been furnished under Sect. 2 (5) of the dyestuff dianisidine \sQ the pyrazolone from dehydrothiotoluidine. Pyrazolones derived from aminoarylthiazoles are made by diazotizing monoaminoarylthiazoles, reducing to the corresponding hydrazines and condensing with an acylacetic acid ester, e.g. aceto, benzoyl or oxal acetic acid esters. Examples are given. Specification 26236/13, [Class 2 (iii)], is referred to.
GB3904/33A 1932-02-08 1933-02-08 Process for the manufacture of azodyestuffs and intermediate products therefor Expired GB414684A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE414684X 1932-02-08

Publications (1)

Publication Number Publication Date
GB414684A true GB414684A (en) 1934-08-08

Family

ID=6448387

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3904/33A Expired GB414684A (en) 1932-02-08 1933-02-08 Process for the manufacture of azodyestuffs and intermediate products therefor

Country Status (1)

Country Link
GB (1) GB414684A (en)

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