GB302599A - Manufacture of azo-dyestuffs insoluble in water - Google Patents

Manufacture of azo-dyestuffs insoluble in water

Info

Publication number
GB302599A
GB302599A GB37253/28A GB3725328A GB302599A GB 302599 A GB302599 A GB 302599A GB 37253/28 A GB37253/28 A GB 37253/28A GB 3725328 A GB3725328 A GB 3725328A GB 302599 A GB302599 A GB 302599A
Authority
GB
United Kingdom
Prior art keywords
chloro
oxynaphthoic acid
anisidide
aminotoluene
grounding
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
GB37253/28A
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 GB302599A publication Critical patent/GB302599A/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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

302,599. I. G. Farbenindustrie Akt.- Ges. Dec. 17, 1927, [Convention date]. Azo dyes.-Azo dyes, insoluble in water and of good fastness to light, are produced in substance or on the fibre by coupling with arylides of 2 : 3- oxynaphthoic acid diazotized dihalogen-2-aminotoluenes carrying one halogen in 4-position and carrying at least one bromine atom. The following examples are specified : (1) Well-boiled cotton yarn is dyed a vivid bluish red, very fast to light, by impregnating in a grounding liquor containing the 2<1> : 5<1>-dimethoxyanilide of 2 : 3-oxynaphthoic acid and developing with diazotized 4-chloro-5- bromo-2-aminotoluene. (2) A similar bluish red dyeing is obtained by grounding with the 2<1>- or 4<1>-anisidide of 2 : 3-oxynaphthoic acid and developing as in (1), and a similar dull alizarin red dyeing is obtained by grounding with the 5<1>- chloro-2<1>-anisidide of 2 : 3-oxynaphthoic acid and developing as in (1). (3) A bluish red dyeing is obtained by grounding with the 51-chloro-21- anisidide of 2: 3-oxynaphthoic acid and developing with diazotized 4: 5-dibromo-2-aminotoluene, and a vivid yellowish red by grounding with the 2'- or 4<1>-anisidide or the 2<1> : 5<1>-dimethoxyanilide of 2 : 3-oxynaphthoic acid and developing similarly. (4) The bluish red dyestuff 4-chloro-5- bromo-2-aminotoluene # the 4'-anisidide of 2 : 3-oxynaphthoic acid is produced in substance. Specifications 6379/12, and 17279/13, [Class 15 (ii), Dyeing, Processes &c. for], are referred to. 5-Bromo-4-chloro-2-amitotoluene is obtained by acetylating 4-chloro-2-aminotoluene by means of acetic anhydride, brominating the product, and saponifying to remove the acetyl group. The Specification as open to inspection under Sect. 91 (3) (a) comprises also the use as diazo component of any dihalogen-2-aminotoluene carrying one halogen in 4-position and carrying at least one halogen atom other than chlorine. This subject-matter does not appear in the Specification as accepted.
GB37253/28A 1927-12-17 1928-12-17 Manufacture of azo-dyestuffs insoluble in water Expired GB302599A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE302599X 1927-12-17

Publications (1)

Publication Number Publication Date
GB302599A true GB302599A (en) 1929-11-28

Family

ID=6106791

Family Applications (1)

Application Number Title Priority Date Filing Date
GB37253/28A Expired GB302599A (en) 1927-12-17 1928-12-17 Manufacture of azo-dyestuffs insoluble in water

Country Status (1)

Country Link
GB (1) GB302599A (en)

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