GB348811A - Manufacture of azo-dyestuffs insoluble in water - Google Patents

Manufacture of azo-dyestuffs insoluble in water

Info

Publication number
GB348811A
GB348811A GB1058530A GB1058530A GB348811A GB 348811 A GB348811 A GB 348811A GB 1058530 A GB1058530 A GB 1058530A GB 1058530 A GB1058530 A GB 1058530A GB 348811 A GB348811 A GB 348811A
Authority
GB
United Kingdom
Prior art keywords
amino
chloro
dyes
trimethylbenzene
class
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
GB1058530A
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 GB1058530A priority Critical patent/GB348811A/en
Publication of GB348811A publication Critical patent/GB348811A/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

Azo dyes; azo dyes, forming on the material.-Azo dyes are made in substance or on a substratum by coupling a diazotized 1-amino-2 : 3-trimethylbenzene halogenated in the 4-position with an arylide of 2 : 3-oxynaphthoic acid, free from groups rendering the dyestuffs soluble in water. In examples (1) cotton impregnated with 2 : 3-oxynaphthoyl - 11 - amino - 21 - methoxy - 41-chlorobenzene is developed with diazotized 1-amino-4 chloro-2 : 3 : 5-trimethylbenzene; a fast vivid blueish Turkey red is obtained, (2) using 2 : 3-oxynaphthoyl - 11 - amino - 41 - chloro-21 : 51-dimethoxybenzene (Specification 331,247, [Class 2 (iii), Dyes &c.], as in (1) a vivid clear Turkey red is obtained, (3) diazotized 1-amino-4-chloro-2 : 3 : 5-trimethylbenzene is coupled with 2 : 3-oxynaphthoyl-11-amino-21 : 51-dimethoxybenzene. Other diazo components specified are the 4-bromo- and 4-iododerivatives and other coupling components the 2 : 3-oxynaphthoyl derivatives of o-toluidine, o-anisidine, 1-amino-2-methyl-4-chlorobenzene, 1-amino-2-methoxy-5-chlorobenzene, 1-amino-2 : 3-dimethoxybenzene, 1-amino-4-chloro-2 : 3 : 5-trimethylbenzene, 1-amino-4-chloro-2 : 5-diethoxybenzene (Specification 332,932, [Class 2 (iii), Dyes &c.]), 1-amino-4-chloro-3-methyl-6-methoxybenzene, a - and b -naphthylamine, 1-amino-4-methoxynaphthalene, (Specification 306,415, [Class 2 (iii), Dyes &c.]), 2-amino-3-methoxynaphthalene (Specification 309,879, [Class 2 (iii), Dyes &c.]), and o-phenetidine. Specifications 6379/12 and 17279/13, [both in Class 2 (iii), Dyes &c.], also are referred to. 1-Amino-4-halogen-2 : 3 : 5-trimethylbenzenes are made by the chlorination, bromination, and iodination respectively of 1-amino-2 : 3 : 5-trimethylbenzene. Arylides of 2 : 3-oxynaphthoic acid.-The arylides specified are made from 2 : 3-oxynaphthoic acid and the corresponding base. 1-Amino - 4 - chloro-2 : 5-diethoxybenzene is made by reducing 1 - nitro - 2 : 5 - diethoxybenzene and chlorinating.
GB1058530A 1930-04-03 1930-04-03 Manufacture of azo-dyestuffs insoluble in water Expired GB348811A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1058530A GB348811A (en) 1930-04-03 1930-04-03 Manufacture of azo-dyestuffs insoluble in water

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1058530A GB348811A (en) 1930-04-03 1930-04-03 Manufacture of azo-dyestuffs insoluble in water

Publications (1)

Publication Number Publication Date
GB348811A true GB348811A (en) 1931-05-21

Family

ID=9970537

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1058530A Expired GB348811A (en) 1930-04-03 1930-04-03 Manufacture of azo-dyestuffs insoluble in water

Country Status (1)

Country Link
GB (1) GB348811A (en)

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