GB462629A - Manufacture of dyestuffs - Google Patents

Manufacture of dyestuffs

Info

Publication number
GB462629A
GB462629A GB5910/36A GB591036A GB462629A GB 462629 A GB462629 A GB 462629A GB 5910/36 A GB5910/36 A GB 5910/36A GB 591036 A GB591036 A GB 591036A GB 462629 A GB462629 A GB 462629A
Authority
GB
United Kingdom
Prior art keywords
acid
amino
sulphone
nitrophenyl
wool
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
GB5910/36A
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 GB462629A publication Critical patent/GB462629A/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
    • C09B29/24Monoazo dyes prepared by diazotising and coupling from coupling components containing both hydroxyl and amino directing groups
    • C09B29/28Amino naphthols
    • C09B29/30Amino naphtholsulfonic acid

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Azo dyes; acid wool dyes without mordants, dyeing with.--Azo dyestuffs are manufactured by coupling a diazo-compound with an aldehyde bisulphite compound of 2-amino-8-naphthol-6-sulphonic acid in alkaline, neutral or acid medium. Suitable diazo components are aniline, toluidines, anisidines and sulphonic acids thereof, their substitution products containing a nitro-group in p-position to the amino-group, and particularly compounds nitrated in p-position to the amino-group and containing in o-position a sulphone-alkyl or -aralkyl group, e.g. 1-amino-4-nitrophenyl-2-methyl, -ethyl or benzyl sulphone, or substitution products thereof, e.g. those containing halogen, alkyl, alkoxy or nitro-groups. The products dye animal fibres, e.g. wool and silk, advantageously in the presence of sulphuric acid or of capillary active substances containing in their kation a basic nitrogen atom and an aliphatic or araliphatic residue of more than 8 carbon atoms. Examples describe the manufacture of the following dyestuffs: (1) 1-amino-4-nitrophenyl-2-methyl sulphone --> the sodium salt of the formaldehyde bisulphite compound of 2 : 8 : 6-acid; the product dyes wool or silk in an acid bath blue shades; (2) 1-amino-4-nitrophenyl-2-benzyl sulphone --> the same coupling component or the corresponding potassium or other salt (somewhat more greenish-blue shades); the diazo-component may be replaced by the 2-ethyl sulphone, by nitrated amines such as p-nitraniline or p-nitro-o-chloraniline (violet shades), by p - nitraniline - o - sulphonic acid (reddish-blue shades), or by simpler amines such as aniline, sulphanilic acid, naphthionic acid or monobenzoyl - p - phenylenediamine (orange to red); the coupling component may be replaced by the corresponding acetaldehyde or furfural bisulphite compound. In example (3), wool is dyed blue with the product of (1) from a bath containing sodium sulphate and sulphuric acid. Specifications 11343/99, [Class 2], 433,230, 436,790, 436,863, 439,890, and 451,970 are referred to. Aldehyde bisulphite compounds of 2 : 8 : 6-acid are manufactured by reacting the acid or a salt thereof with an aldehyde bisulphite compound. 1-Amino-4-nitrophenyl-2-methyl, -ethyl and benzyl sulphones are obtainable by reacting sodium 1 - chloro - 4 - nitrobenzene - 2 - sulphinate with methyl bromide, ethyl bromide or benzyl chloride respectively, and heating the products with aqueous ammonia under pressure.
GB5910/36A 1935-02-28 1936-02-27 Manufacture of dyestuffs Expired GB462629A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH462629X 1935-02-28

Publications (1)

Publication Number Publication Date
GB462629A true GB462629A (en) 1937-03-12

Family

ID=4515767

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5910/36A Expired GB462629A (en) 1935-02-28 1936-02-27 Manufacture of dyestuffs

Country Status (1)

Country Link
GB (1) GB462629A (en)

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