发明名称 Polyazo dyestuffs and process for their manufacture
摘要 536,159. Dyes. GEIGY AKT.-GES., J. R. Feb. 14, 1940, No. 2824. Convention date, Feb. 15, 1939. [Class 2 (iii)] Polyazo dyes, giving full level brown dyeings, specially fast to polishing, on leather and of the general formula wherein A represents the residue of 3-hydroxydiphenylamine or a derivative thereof capable of coupling twice in alkaline medium, B represents the residue of a 1: 8 - aminonaphtholmono-or-di-sulphonic acid coupled in alkaline medium, C and D represent the residues of the same or different diazo or diazoazo compounds, preferably substituted by nitro groups, the finished dyestuff containing at least 2 sulphonic groups, are obtained by (a) coupling in alkaline medium the diazotized 1 : 8- aminonaphtholsulphonic acid (1 mol.) with 3 - hydroxydiphenylamine or its derivative (1 mol.) and coupling the product in alkaline medium successively with the 2 mols. of the diazotized amine (or amines) and/or aminoazo compound (or compounds), (b) coupling in alkaline medium a diazotized amine or aminoazo compound ( 1 mol. ) with the 1: 8 - aminonaphtholsulphonic acid (1mol.), diazotizing and coupling in alkaline medium with the 3 - hydroxydiphenylamine or its derivative (1 mol.) and coupling the product in alkaline medium with a diazotized amine or aminoazo compound (1 mol.). Examples relate to the production of the dyestuffs, (1) sulphanilic acid - (alkaline) 1 : 8-aminonaphthol-3: 6-disulphonic acid # (alkaline) 3-hydroxydiphenylamine or its 2<SP>1</SP>-, 3<SP>1</SP>- or 4'-methyl derivative (alkaline) # 4-nitroaniline by method (a); (2) 4-nitroaniline, or its 2-sulphonic acid # (alkaline) 1 : 8 - aminonaphthol-3: 6 - disulphonic acid # (alkaline) 3-hydroxy-2<SP>1</SP>-methyldiphenylamine (alkaline) # 4<SP>1</SP>-amino-4-nitrodiphenylamine-2-sulphonic acid or 4 - nitroaniline (# Cleve's acid, if desired) by method (a); (3) sulphanilic acid # (alkaline) 1 : 8 - amiinonaphthol- 3 : 6-disulphonic acid # (alkaline) 3-hydroxy-2<SP>1</SP>-methyldiphenylamine #naphthionic acid by method (a), the naphthionic acid may be replaced by one of the aminoazo compounds naphthionic or sulphanilic acid or 4-nitroaniline # Cleve's acid ; (4) 4- nitroaniline or sulphanilic acid or 4<SP>1</SP> - amino- 4-nitrodiphenylamine- 2 - sulphonic # (alkaline) 1: 8 aminonaphthol - 3 : 6 - disulphonic acid - (alkaline) 3-hydroxy-2'-methyldiphenylamine (alkaline) #(Cleve's acid, if desired #) 4<SP>1</SP>-amino - 4 - nitrodiphenylamine - 2 - sulphonic acid, by method (b). Other specified derivatives of 3 - hydroxydiphenylamine are the 2<SP>1</SP>-and 4<SP>1</SP>-chloro- and the 2<SP>1</SP>- and 4<SP>1</SP>-methoxy- and ethoxyderivatives. The use of the 1:8:4-acid as the 1:8- aminonaphtholsulphonic acid is also specified. Specification 251,140, [Class 2 (iii)], is referred to. 2 1 and 4 <SP>1</SP>- chloro-, methoxy- and, ethoxy derivatives of 3 - hydroxydiphenylamine are obtained by heating the 2<SP>1</SP>- and 4<SP>1</SP>-chloranilines, anisidines and phenetidines respectively with resorcinol in presence of boric acids. The Specification as open to inspection under Sect. 91 comprises also the manufacture of the dyestuffs by (c) coupling a diazotized amine or aminoazo compound (1 mol.) with the 3- hydroxydiphenylamine or its derivative (1 mol.) coupling with the diazotized 1 :8 - aminonaphtholsulphonic acid (1 mol.) and coupling the product with a diazotized amine or aminoazo compound (1 mol.), and (d) coupling in alkaline medium a diazotized amine or aminoazo compound (1 mol.) with the 1 : 8-aminonaphtholsulphonic acid (1 mol.), diazotizing the product and coupling with the mono-or dis-azo dyestuff obtained by coupling a diazotized amine or aminoazo compound (1 mol.) with the 3- hydroxydiphenylamine or its derivative (1 mol.). Additional examples (5) and (6) illustrating process (c) and (d) respectively relate to the production of the dyestuffs, 4-nitroaniline or 4<SP>1</SP>- amino - 4 - nitrodiphenylamine - 2 - sulphonic acid - (alkaline) 1 : 8 - aminonaphthol-3: 6- or (in (5)) 4 : 6- or 2 : 4-disulphonic acid # 3- hydroxy-2<SP>1</SP>-methyldiphenylamine # sulphanilic or (in (6)) naphthionic acid. This subjectmatter does not appear in the Specification as accepted.
申请公布号 US2276169(A) 申请公布日期 1942.03.10
申请号 US19400318182 申请日期 1940.02.09
申请人 THE FIRM J. R. GEIGY A. G. 发明人 DOBLER FRITZ;BUESS HANS
分类号 C09B33/18;C09B33/22;C09B35/44 主分类号 C09B33/18
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