GB537831A - Manufacture of azo-dyestuffs - Google Patents

Manufacture of azo-dyestuffs

Info

Publication number
GB537831A
GB537831A GB304/40A GB30440A GB537831A GB 537831 A GB537831 A GB 537831A GB 304/40 A GB304/40 A GB 304/40A GB 30440 A GB30440 A GB 30440A GB 537831 A GB537831 A GB 537831A
Authority
GB
United Kingdom
Prior art keywords
aniline
acid
nitroaniline
nitrated
dimethylaniline
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
GB304/40A
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.)
BASF Schweiz AG
Original Assignee
Gesellschaft fuer Chemische Industrie in Basel CIBA
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 Gesellschaft fuer Chemische Industrie in Basel CIBA filed Critical Gesellschaft fuer Chemische Industrie in Basel CIBA
Publication of GB537831A publication Critical patent/GB537831A/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
    • C09B43/00Preparation of azo dyes from other azo compounds
    • C09B43/04Preparation of azo dyes from other azo compounds by nitration

Landscapes

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

Abstract

537,831. Dyes.. SOC. OF CHEMICAL INDUSTRY IN BASLE. Jan. 5, 1940, Nos. 304 and 305. Convention dates, Jan. 5, 1939 and Dec. 4, 1939. [Classes 2 (iii) and 15 (ii)] Monoazo dyes, free from sulphonic acid groups and of the general formula wherein A and B represent nuclei of the benzene series, y and z each represent H, alkyl or substituted alkyl, the nucleus A carries at least one substituent capable of enhancing the acidity of a phenolic hydroxy group and the amino group is in p-position to the azo group. Specified acidity-enhancing substituents are halogen atoms and nitro, cyano, sulphone, sulphonamide, carboxyl, ketone and carboxylic amide groups. Specified aminoazo dyestuffs used as starting materials are 4-nitroaniline # aniline, N-dimethyl-, N- diethyl-, N-methyl-, N-ethyl- or N-methyl N-butyl-aniline, 2-toluidine, 2-anisidine, 3- chloraniline or 3- chloro-N-dimethyl-aniline ; 3- nitroanilineaniline, 2-toluidine or 2-anisidine ; 2-nitro-aniline # aniline, N - dimethylaniline or 2-toluidine; 3-nitro-2-aminotoluene # aniline ; 2-, 3- or 4-chloroanilineaniline; aniline-2-, 3- or 4-methylsulphone # aniline ; aniline-3- methylsulphone # N - dimethylaniline ; 4- nitro-2-chloroaniline or 2 : 5-dichloroaniline # aniline or N-dimethylaniline ; 2 : 6-dichloro-4- nitroaniline # N - dimethylaniline ; 3 - nitro - 5 - chloroaniline, 2 : 4 - dinitroaniline, 2 : 4 - dinitro - 6 - chloroaniline or 4 - cyanoaniline # aniline ; 4 - cyanoaniline # N - dimethylaniline ; aniline - 4 - sulphodimethylamide or aniline - 4 - carboxylic acid or its ethylamide # aniline ; 2 - nitroaniline - N - ethyl - N - # - hydroxyethyl - aniline ; 3 - nitroaniline # N - di(#-hydroxyethyl)aniline; N-di (#-hydroxyethyl) - 3 - toluidine ; N - ethyl - N - # - chlorethyl - aniline or N - ethyl - N - # - methoxyethyl - aniline ; 4 - nitroaniline # N - ethyl - N - # - hydroxyethyl - aniline. The nitration may be effected by treatment with conc. or dilute nitric acid, especially in presence of sulphuric, glacial acetic or chlorosulphonic acid or of acetic anhydride, a halogenated hydrocarbon or dioxane ; primary or secondary amino groups in the starting materials may be acidylated before or after the nitration. The products containing diazotizable amino groups may be diazotized and further coupled with components in substance or on the fibre. In examples, (1) the dyestuff, 4-nitroaniline # aniline, is nitrated at or below 0‹ C. with cone. nitric acid in conc. sulphuric acid ; the neutralized product may be dispersed, e.g. with turkey red oil or sulphite cellulose liquor for dyeing acetate artificial silk full reddish yellow shades, fast to light ; the dyestuff, 4-chloroaniline # aniline (coupled as the #- methanesulphonic acid and hydrolysed may be similarly nitrated or may be first acetylated and then nitrated in sulphuric acid, dioxane, tetrachlorethane or glacial acetic acid ; (2) the dyestuff, 3-nitro-2-aminotolueneaniline, is nitrated at 0-10‹ C. in conc. sulphuric acid ; the neutralized product dyes acetate artificial silk brown-yellow ; the dyestuffs, 2-nitroaniline # - N-dimethyl- or N-ethyl-N-#-hydroxyethyl-aniline may be similarly nitrated ; in the latter case the hydroxy group may be converted into the sulphuric acid ester group before nitration, with or without subsequent saponification to restore the hydroxy group ; (3) the dyestuff, 4 - nitro - 2 - chloro - or 2 : 6 -dichloro - aniline - aniline, is similarly nitrated in conc. sulphuric acid ; the neutralized products dye acetate artificial silk yellow ; (4) the dyestuff, 3-nitroaniline # aniline, is similarly nitrated in sulphuric acid ; the product, neutralized if desired, dyes acetate artificial silk yellow ; a similar product is obtainable by acetylating the parent dyestuff with acetic anhydride, nitrating the acetylation product with nitric acid in glacial acetic acid and saponifying to the acetyl group ; (5) the dyestuff 3- or 4- nitroaniline # N-dimethylaniline, is nitrated at about 10‹ C. with nitric acid in conc. sulphuric acid or with nitrosyl chloride in tetrachlorethane ; the neutralized products due acetate artificial silk brown ; (6) the dyestuff, 4-chloroanilineaniline, is nitrated at about 0‹ C. with nitric acid in conc. sulphuric acid ; the neutralized product dyes acetate artificial silk yellow ; the dyestuffs, aniline-2- or 4-methylsulphone # aniline or aniline-3-methylsulphone # N-dimethylaniline may be similarly nitrated ; the similarly nitrated products from the dyestuffs 4-nitroaniline- 2-anisidine or 3-chloro- N-dimethylaniline, dye acetate artificial silk orange to red ; (7) acetate artificial silk yarn is dyed a brilliant yellow by treatment in a soap solution, heated during ¥ hour to 80-85‹ C. and so maintained for a further “ hour. containing the dyestuff of (1) above dispersed with Turkey red oil, sulphite cellulose liquor or a sulphonated residue from the manufacture of benzaldehyde. The Specification as open to inspection under Sect. 91 comprises also the nitration of the dyestuffs of the above general formula containing sulphonic groups, such as sulphanilic acid # aniline or N-dimethylaniline and 4-nitroaniline-2-sulphonic acid- N-diethylaniline, the products being suitable for dyeing wool and silk. This subject-matter does not appear in the Specification as accepted.
GB304/40A 1939-01-05 1940-01-05 Manufacture of azo-dyestuffs Expired GB537831A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH537831X 1939-01-05

Publications (1)

Publication Number Publication Date
GB537831A true GB537831A (en) 1941-07-08

Family

ID=4518878

Family Applications (1)

Application Number Title Priority Date Filing Date
GB304/40A Expired GB537831A (en) 1939-01-05 1940-01-05 Manufacture of azo-dyestuffs

Country Status (1)

Country Link
GB (1) GB537831A (en)

Similar Documents

Publication Publication Date Title
US2373700A (en) Azo compounds and material colored therewith
US2359305A (en) Azo compounds and material colored therewith
GB537831A (en) Manufacture of azo-dyestuffs
US2824096A (en) Tricyanovinylaryleneazoarylene compounds
US2336275A (en) Azo dye compound
US2311033A (en) Azo compounds and material colored therewith
US2289414A (en) Azo dye and coloration of cellulose derivatives therewith
US2249774A (en) Azo compound and material colored therewith
US2231707A (en) Azo compounds and material colored therewith
US2420008A (en) Disazo dyes containing higher acylamino group
GB957419A (en) Benzene monoazo dyestuffs
US3717626A (en) Water-insoluble phenyl-azo-phenyl dyestuffs
GB523304A (en) Improvements in or relating to colouring cellulose ester or ether materials
GB794135A (en) Water-insoluble monoazo dyestuffs containing cyanogen groups
GB584731A (en) Manufacture of new azo-dyestuffs
GB587467A (en) Manufacture of new azo-dyestuffs
GB560298A (en) Dyes and dyeing
GB298518A (en) Process for the manufacture of polyazo dyestuffs
GB246394A (en) Manufacture of new dyestuffs
GB372562A (en) Process for the manufacture of azo dyestuffs
GB623763A (en) Process for the production of monazo dyes containing 6-ethyl and 6-propyl pyronone couplers
GB395005A (en) New disazo dyestuffs and their application
GB462176A (en) Manufacture of azo dyestuffs
GB510091A (en) Manufacture of azo-dyestuff derivatives
GB549709A (en) Manufacture of monoazo dyestuffs, and their use and the dyed products