Sulfaphenyl-azo-phenyl-azo-aminophenyl dyestuffs

Description

The subject-matter of the present invention comprises new valuable disazo dyestuffs which in the form of the free acid correspond to the general formula ##STR4## as well as their production and their use for the dyeing of synthetic fibre materials, especially those of polyamides.
In the general formula (I) ##STR5##
In the radicals (Ia) and (IIa)
R.sub.1 stands for hydrogen, an alkyl radical or a phenyl group;
R.sub.2 and R.sub.3, independently of one another, stand for hydrogen, halogen, an alkyl group, an alkoxy group or an acylamino group;
R.sub.4 means hydrogen, halogen, an alkyl group, an alkoxy group or an acylamino group;
R.sub.5 stands for hydrogen, an alkyl group or an alkoxy group;
R.sub.6 and R.sub.7, independently of one another, stand for hydrogen, hydroxy, cyano, halogen, acyloxy, alkoxy-carbonyl or phenyl;
X means an alkylene radical with 1 - 4 carbon atoms;
R.sub.8 means an alkyl, phenyl, 2-naphthyl or 4-biphenylyl group which is not further substituted;
R.sub.9 means hydrogen or an alkyl group with 1 - 6 carbon atoms which may be substituted by a nitrile, carboxamide or carboxyl group;
R.sub.10 stands for a substituent; and
n stands for the numbers 0 - 2.
The alkyl and alkoxy radicals as well as the phenyl radicals may be further substituted, unless otherwise stated.
Preferred alkyl and alkoxy radicals R.sub.1 - R.sub.5 are those with 1 - 4 carbon atoms.
The following radicals may be mentioned by way of example: --CH.sub.3, --C.sub.2 H.sub.5, --C.sub.3 H.sub.7, --C.sub.4 H.sub.9, --OCH.sub.3, --OC.sub.2 H.sub.5, --OC.sub.4 H.sub.9.
Suitable halogen atoms are primarily Cl and Br.
Suitable phenyl radicals are primarily phenyl, chlorophenyl, nitrophenyl, C.sub.1 -C.sub.4 -alkoxyphenyl.
The acylamino groups primarily comprise formylamino, alkyl-carbonylamino, phenyl-carbonylamino, alkyl-sulphonylamino and phenyl-sulphonylamino groups; the alkyl and phenyl radicals may be further substituted.
Suitable acylamino groups are, for example, formylamino, acetylamino, propionylamino, butyrylamino, methylsulphonylamino, phenylsulphonylamino, hydroxyacetylamino, phenoxyacetylamino, p-chlorobenzoylamino, benzoylamino, 2,5-dichlorobenzoylamino, phenylacetylamino radicals.
The acyloxy groups primarily comprise alkyl-carbonyloxy groups with 1 - 4 carbon atoms in the alkyl group and alkoxy-carbonyloxy groups with 1 - 4 carbon atoms in the alkoxy group.
Suitable alkoxy-carbonyloxy groups are primarily those with 1 - 4 carbon atoms in the alkoxy group.
Suitable alkylene radicals X are, for example, --CH.sub.2 --, --CH.sub.2 CH.sub.2 --, ##STR6## --CH.sub.2 --CH.sub.2 --CH.sub.2 --CH.sub.2 --.
Suitable radicals --X--R.sub.6 or --X--R.sub.7 are, for example, --CH.sub.3, --C.sub.2 H.sub.5, --C.sub.4 H.sub.9, --CH.sub.2 CH.sub.2 CN, --CH.sub.2 CH.sub.2 OH, --CH.sub.2 CH.sub.2 OCOCH.sub.3, --CH.sub.2 CH.sub.2 OCOC.sub.2 H.sub.5, --CH.sub.2 CH.sub.2 OCOC.sub.3 H.sub.7, --CH.sub.2 CH.sub.2 OCOOCH.sub.3, --CH.sub.2 CH.sub.2 OCOOC.sub.2 H.sub.5, --CH.sub.2 CH.sub.2 OCOOC.sub.4 H.sub.9, --CH.sub.2 --C.sub.6 H.sub.5, --CH.sub.2 CH.sub.2 Cl, --CH.sub.2 CH.sub.2 COOCH.sub.3, --CH.sub.2 CH.sub.2 COOC.sub.2 H.sub.5.
Preferred dyestuffs are those of the general formula ##STR7## in which R.sub.1 - R.sub.7 and X have the same meaning as in formula (I), and, more particularly, those of the formula ##STR8## in which R.sub.1 ' stands for alkyl with 1 - 4 carbon atoms;
R.sub.2 ' means hydrogen or alkoxy with 1 - 4 carbon atoms;
R.sub.3 ' stands for hydrogen or alkyl with 1 - 4 carbon atoms;
R.sub.4 ' means hydrogen, alkyl with 1 - 4 carbon atoms, Cl, Br or an alkyl-carbonylamino group with 1 - 4 carbon atoms;
R.sub.5 ' means hydrogen or alkoxy with 1 - 4 carbon atoms;
X means --CH.sub.2 CH.sub.2 -- or --CH.sub.2 --; and
R.sub.6 ' and R.sub.7 ' independently of one another, stand for hydrogen, Cl, OH, CN, alkyl-carbonyloxy with 1 - 4 carbon atoms in the alkyl group, or alkoxy-carbonyl with 1 - 4 carbon atoms in the alkoxy group.
Other preferred dyestuffs are those of the general formula ##STR9## in which R.sub.1 - R.sub.3 as well as R.sub.8 and R.sub.9 have the same meaning as in formula (I),
and, more particularly, those of the formula ##STR10## in which R.sub.1 ' stands for alkyl with 1 - 4 carbon atoms;
R.sub.2 ' means hydrogen or alkoxy with 1 - 4 carbon atoms;
R.sub.3 ' stands for hydrogen or alkyl with 1 - 4 carbon atoms;
R.sub.8 ' stands for alkyl with 1 - 4 carbon atoms or for phenyl;
R.sub.9 ' means hydrogen or an alkyl group with 1 - 4 carbon atoms which may be substituted by a nitrile, carboxamide or carboxyl group.
The new dyestuffs are obtained by diazotising aniline-sulphonic acids of the formula ##STR11## in which R.sub.1 has the same meaning as in formula (I); combining the product with coupling components of the general formula ##STR12## in which R.sub.2 and R.sub.3 have the same meaning as in formula (I) and Z stands for H or for the radical of a group which can be split off and facilitates the coupling, for example, a sulphoalkylene group or a sulphonic acid group;
further diazotising the resultant monoazo dyestuffs of the formula ##STR13## and coupling with an amine of the formula ##STR14## or an indole of the formula ##STR15## in which R.sub.4 - R.sub.10, n and X have the same meaning as in formula (I).
In the case where Z is different from H, the group --NHZ is converted into a group NH.sub.2 prior to diazotisation.
The dyestuffs according to the invention can also be synthetised by diazotising a middle component ##STR16## in which R.sub.2 and R.sub.3 have the same meaning as above and acyl represents an acyl radical, for example, an acetyl, oxalyl or benzoyl radical;
coupling in an alkaline medium with phenol-2- or -3-sulphonic acid to form dyestuffs of the formula ##STR17## subsequently alkylating the hydroxyl group, if desired; eliminating the acyl radical from the dyestuffs (X) or reducing the nitro group in the dyestuffs (XI) to the amino group; subsequently diazotising the aminoazo dyestuff of the formula ##STR18## and coupling, as described above, with amines of the formula (VII) or with indoles of the formula (VIIa).
Suitable aniline-sulphonic acids (IV) are, for example; 4-methoxy-aniline-sulphonic acid-(3), 4-methoxy-aniline-sulphonic acid-(2), 4-ethoxy-aniline-sulphonic acid-(3), 4-ethoxy-aniline-sulphonic acid-(2), 4-propoxy-aniline-sulphonic acid-(3), 4-isopropoxy-aniline-sulphonic acid-(2), 4-butoxy-aniline-sulphonic acid-(3), 4-isobutoxy-aniline-sulphonic acid-(2), 4-tert.-butoxyaniline-sulphonic acid-(3), 4-hydroxy-aniline-sulphonic acid-(3), 4-phenoxy-aniline-sulphonic acid-(3).
Suitable coupling components of the general formula (V) are, for example:
aniline-.omega.-methane-sulphonic acid or aniline-sulphamic acid, 2-aminotoluene, 3-aminotoluene, 2-amino-ethylbenzene, 3-amino-ethylbenzene, 3-chloroaniline, 3-bromoaniline, 2-amino-anisole, 3-amino-anisole, 2-amino-ethoxybenzene, 3-amino-ethoxybenzene, 1 -amino-2,5-dimethylbenzene, 1-amino-2,3-dimethyl-benzene, 1-amino-3,5-dimethylbenzene, 3-amino-4-methoxy-toluene, 2-amino-4-methoxy-toluene, 2-amino-1,4-dimethoxy-benzene, 2-amino-4-ethoxy-toluene, 2-amino-1,4-diethoxybenzene, 3-acetylamino-aniline, 3-propionylamino-aniline.
Suitable coupling components of the general formula (VII) or (VIIa) are, for example:
N,n-dimethylaniline, N,N-diethylaniline, N-methyl-N-n-butyl-aniline, N,N-diethyl-m-toluidine, N,N-diethylamino-3-chlorobenzene, N,N-diethyl-N'-formyl-m-phenylene-diamine, N,N-diethyl-N'-acetyl-m-phenylene-diamine, N,N-diethyl-N'-propionyl-m-phenylene-diamine, N,N-diethylamino-3-methoxybenzene, 1-N,N-diethylamino-2,5-dimethoxybenzene, 1-N,N-diethylamino-2,5-diethoxybenzene, 1-N,N-diethylamino-2-methoxy-3-acetylaminobenzene, N-ethyl-N-.beta.-chloroethyl-aniline, N,N-bis-(.beta.-chloro-ethyl)-aniline, N-(.beta.-chloroethyl)-N-butyl-aniline, N-(.beta.-chloroethyl)-N-ethyl-m-toluidine, N,N-bis-(.beta.-chloroethyl)-m-toluidine, N-methyl-N-.beta.-hydroxyethyl-aniline, N-ethyl-N-.beta.-hydroxyethylaniline, N,N-bis-(.beta.-hydroxyethyl)-aniline, N-butyl-N-(.beta.-hydroxyethyl)-aniline, N,N-bis-(.beta.,.gamma.-dihydroxypropyl)-aniline, N-ethyl-N-benzyl-aniline, N-ethyl-N-benzyl-m-toluidine, N-ethyl-N-.beta.-hydroxyethyl-m-toluidine, N,N-bis-(.beta.-hydroxyethyl)-m-toluidine, 1-(N-ethyl-N-.beta.-hydroxyethyl)-amino-2-methoxy-5-methylbenzene, N-ethyl-N-.beta.-hydroxyethyl-N'-acetyl-m-phenylenediamine, N,N-bis-(.beta.-hydroxyethyl)-N'-acetyl-m-phenylene-diamine, 1-N,N-bis-(.beta.-hydroxyethyl)-amino-2-methoxy-5-acetylaminobenzene, 1-N,N-bis-(.beta.-hydroxyethyl)-amino-2-ethoxy-5-acetylamino-benzene, 1-N,N-bis-(.beta.-hydroxyethyl)-amino-2-methoxy-5-propionylamino-benzene, N-ethyl-N-.beta.-acetoxyethylaniline, N,N-bis-(.beta. -acetoxyethyl)-aniline, N-butyl-N-.beta.-acetoxyethyl-aniline, N-ethyl-N-.beta.-acetoxyethyl-m-toluidine, N,N-bis-(.beta.-acetoxyethyl)-m-toluidine, 1-(N-ethyl-N-.beta.-acetoxyethyl)-amino-2-methoxy-5-methylbenzene, N-ethyl-N-.beta.-acetoxyethyl-N'-acetyl-m-phenylenediamine, N,N-bis-(.beta.-acetoxyethyl)-N'-acetyl-m-phenylene-diamine, 1-N,N-bis-(.beta.-acetoxyethyl)-amino-2-methoxy-5-acetylamino-benzene, 1-N,N-bis-(.beta.-acetoxyethyl)-amino-2-ethoxy-5-acetylamino-benzene, 1-N,N-(.beta.-acetoxyethyl)-amino-2-methoxy-5-propionylamino-benzene, N,N-bis-(.beta.-ethoxy-carbonyloxy-ethyl)-aniline, N,N-bis-(.beta.-methoxycarbonyloxy-ethyl)-aniline, N,N-bis-(.beta.-ethoxy-carbonyloxy-ethyl)-m-toluidine, N,N-bis-(.beta.-methoxy-carbonyloxy-ethyl)-m-toluidine, N,N-bis-(.beta.-ethoxy-carbonyloxy-ethyl)-N'-acetyl-m-phenylene-diamine, N,N-bis-(.beta.-methoxy-carbonyloxy-ethyl)-N' -acetyl-m-phenylene-diamine, 1-N,N-bis-(.beta.-ethoxy-carbonyloxy-ethyl)-amino-2-methoxy-5-acetylaminobenzene, 1-N,N-bis-(.beta.-methoxy-carbonyloxy-ethyl)-amino-2-methoxy-5-acetylaminobenzene, 1-N,N-bis-(.beta.-ethoxy-carbonyloxy-ethyl)-amino-2-ethoxy-5-acetylaminobenzene, 1-N,N-bis-(.beta.-methoxy-carbonyloxy-ethyl)-amino-2-ethoxy-5-acetylaminobenzene, N,N-bis-(.beta.-carbomethoxyethyl)-N'-acetyl-m-phenylene-diamine, N-methyl-N-.beta.-cyanoethylaniline, N,N-bis-(.beta.-cyanoethyl)-aniline, N-ethyl-N-.beta. -cyanoethyl-m-toluidine, N-ethyl-N-.beta.-cyanoethyl-N'-acetylamino-m-phenylenediamine, N-.beta.-hydroxyethyl-N-.beta.-cyanoethyl-aniline, N-.beta.-acetoxyethyl-N-.beta.-cyanoethyl-m-toluidine, N-.beta.-methoxy-carbonyloxyethyl-N-.beta.-cyanoethyl-N'-acetylamino-m-phenylene-diamine, N,N-bis-(.beta.-cyanoethyl)-N'-benzoyl-m-phenylene-diamine, N-.beta.-hydroxyethyl-N-.beta.-cyanoethyl-N'-phenacetyl-m-phenylene-diamine, N,N-diethyl-N'-phenoxyacetyl-m-phenylene-diamine, N-ethyl-N-.beta.-cyanoethyl-N'-phenoxyacetyl-m-phenylene-diamine, N,N-bis-(.beta.-cyanoethyl)-N'-p-chlorobenzoyl-m-phenylene-diamine, 2-methylindole, 2-phenylindole, 1-methyl-2-phenylindole, 1,2-dimethylindole, 1-.beta.-cyanoethyl-2-methylindole, 1-.beta.-cyanoethyl-2-phenylindole, .gamma.-(2-phenylindolyl-1)-propionic acid amide, .gamma.-(2-methylindolyl-1)-propionic acid amide, .gamma.-(2-methylindolyl-1)-propionic acid, 2-.beta.-naphthyl-indole, 2-p-biphenylylindole, 2,5-dimethylindole, 2,4-dimethyl-7-methoxyindole, 2-phenyl-5-ethoxyindole, 2-methyl-5-ethoxyindole, 2-methyl-5-chloroindole, 2-methyl-6-chloroindole, 2-methyl-5-nitroindole, 2-methyl-5-cyanoindole, 2-methyl-7-chloroindole, 2-methyl-5-fluoroindole, 2-methyl-5-bromoindole, 2-methyl-5,7-dichloroindole and 1-cyanoethyl-2,6-dimethylindole.
The diazo components of the formula (IV) are diazotised in known manner, for example, in an acidic aqueous solution with a sodium nitrite solution at 0.degree.- 20.degree. C. and the diazo compound is combined with the coupling components of the formulae (V). Coupling can be carried out in a neutral to strongly acidic, but preferably in a weakly acidic or organicaqueous medium.
Further diazotisation of the aminoazo dyestuffs (VI) or (XII) can be carried out, for example, in an acidic aqueous dispersion with a sodium nitrite solution; the diazotisation temperatures may lie between 0.degree. and 30.degree. C. Furthermore, aminoazo dyestuffs of the formula (XII) can also be indirectly diazotised by dissolving them in an alkaline medium, adding a sodium nitrite solution, and pouring the mixture into aqueous hydrochloric acid or adding hydrochloric acid to the mixture.
Coupling of the diazotised aminoazo dyestuffs (VI) or (XII) with amines (VII) or indoles (VIIa) to form the disazo dyestuffs (I) is likewise carried out in known manner, for example in a neutral or a weakly or strongly acidic aqueous medium or also in an aqueous-organic medium. In general, the disazo dyestuffs of the formula (I) are rather sparingly soluble in an acidic medium and can be isolated by simple filtering off, possibly after the addition of 2- 10% sodium chloride. If the dyestuffs are obtained in an impure state, they can be reprecipitated in known manner from hot water, optionally with the addition of alkali. The more sparingly soluble acidically isolated dyestuffs of the formula (I) can be rendered readily water-soluble by mixing them with salts from strong bases and weak acids, for example, trisodium phosphate, disodium hydrogen phosphate, sodium tetraborate, sodium metaphosphate, sodium metasilicate or sodium carbonate.
The dyestuffs according to the invention are suitable for the dyeing of snythetic fibre materials, especially for the dyeing of polyamide fibres, in level, productive, yellowish red, red and bluish red shades of very good fastness to light. They draw well on polyamide fibres even from a neutral to weakly acidic bath. The polyamide fibres primarily comprise those of synthetic polyamides such as .epsilon.-caprolactam or condensation products of adipic acid and hexamethylene-diamine.

EXAMPLE 1 ##STR19##
20.3 g (0.1 mol) 4-amino-anisole-sulphonic acid-(2) are dissolved in 200 ml of water with a sodium hydroxide solution at pH 7, 6.9 g sodium nitrite are added, the mixture is cooled with ice, and 28 ml of concentrated hydrochloric acid are added at 0- 5.degree. C. After 30 minutes, diazotisation has ended. A solution of 10.7 g (0.1 mol) 3-aminotoluene in 100 ml of water and 5 ml of concentrated hydrochloric acid is then added to the diazo suspension. The mixture is then slowly neutralised at 0.degree.- 10.degree. C. with a concentrated sodium hydroxide solution until the pH value is 6. The dyestuff is salted out with 10% sodium chloride and filtered off with suction.
The aminoazo dyestuff so obtained is dissolved in 300 ml of water at pH 7. 6.9 g sodium nitrite are then added, the mixture is cooled, and 28 ml of concentrated hydrochloric acid are added at 0.degree.- 5.degree. C. After diazotising for one hour, the diazo suspension is poured into a solution of 21.1 g (0.1 mol) N-phenyl-N-ethyl-benzylamine in 500 ml of water and 40 ml of concentrated hydrochloric acid. The pH value is then slowly adjusted to pH 4- 5 with sodium acetate or solution of sodium hydroxide. After coupling, the dyestuff is isolated in the usual way and dried at 90.degree. C. The dyestuff dyes polyamide from a weakly acidic or neutral bath in yellowish scarlet shades of good fastness to light.
Valuable water-soluble disazo dyestuffs which dye polyamide in yellowish red to bluish red shades fast to light are also obtained when the procedure described above is followed, but with the use of the compounds given in Column I as diazo component, those of Column II as middle component and those of Column III as final component.
__________________________________________________________________________ Shade onNo. I II III polyamide__________________________________________________________________________ ##STR20## ##STR21## ##STR22## yellowish red3 " " ##STR23## bluish red4 " " ##STR24## yellowish red5 " " ##STR25## scarlet6 " " ##STR26## bluish red7 " " ##STR27## bluish red8 " " ##STR28## red9 " " ##STR29## yellowish red10 " " ##STR30## red11 " " ##STR31## ruby12 " " ##STR32## bluish red13 " ##STR33## ##STR34## bluish scarlet14 " " ##STR35## red15 " " ##STR36## yellowish scarlet16 " " ##STR37## red17 " " ##STR38## bluish red18 " " ##STR39## yellowish red19 " ##STR40## ##STR41## red20 " ##STR42## ##STR43## yellowish red21 " ##STR44## ##STR45## bluish red22 " ##STR46## ##STR47## bluish red23 ##STR48## ##STR49## ##STR50## red24 " " ##STR51## yellowish scarlet25 " " ##STR52## scarlet26 " " ##STR53## red27 " " ##STR54## red28 " ##STR55## ##STR56## yellowish scarlet29 " " ##STR57## bluish scarlet30 " " ##STR58## yellowish red31 " " ##STR59## red32 " " ##STR60## bluish red33 " " ##STR61## yellowish red34 " " ##STR62## yellowish red35 " " ##STR63## bluish red36 " " ##STR64## red37 " ##STR65## ##STR66## red38 " ##STR67## ##STR68## yellowish red39 " ##STR69## ##STR70## bluish red40 " " ##STR71## bluish red41 " ##STR72## ##STR73## ruby42 ##STR74## ##STR75## ##STR76## yellowish scarlet43 " " ##STR77## red44 " ##STR78## ##STR79## scarlet45 ##STR80## ##STR81## ##STR82## yellowish red46 " ##STR83## ##STR84## red47 ##STR85## ##STR86## ##STR87## red48 " ##STR88## ##STR89## yellowish red49 ##STR90## ##STR91## ##STR92## bluish red50 ##STR93## ##STR94## ##STR95## bluish red51 " " ##STR96## bluish red52 ##STR97## ##STR98## ##STR99## ruby53 " ##STR100## ##STR101## bluish red__________________________________________________________________________
EXAMPLE 54
0.1 mol 4-acetylamino-aniline are diazotised in the usual way and the diazo compound is combined in an alkaline medium with a solution of 0.1 mol phenol-3-sulphonic acid. When the coupling is completed, the resultant monoazo dyestuff is isolated and methylated in the usual way with dimethyl sulphate. The methoxy dyestuff is hydrolysed with a 4% aqueous sodium hydroxide solution for about 1 hour. The resultant aminoazo compound is diazotised at room temperature and the product is coupled with an acidic solution of 0.1 mol N-ethyl-N-phenyl-benzylamine. The product is isolated in the usual way and after drying and pulverising, there is obtained a dyestuff which dyes polyamide from a neutral or weakly acidic bath in scarlet shades.
EXAMPLE 55 ##STR102##
20.3 g (0.1 mol) 4-amino-anisole-sulphonic acid-(2) are dissolved in 200 ml of water with sodium hydroxide at pH 7, 6.9 g sodium nitrite are added, the mixture is cooled with ice and 28 ml of concentrated hydrochloric acid are added at 0.degree.- 5.degree. C. The diazotisation is completed after 30 minutes. A solution of 10.7 g (0.1 mol) 3-amino-toluene in 100 ml of water and 5 ml of concentrated hydrochloric acid is then added to the diazo suspension. The mixture is then slowly buffered at 0.degree.- 10.degree. C. with a concentrated sodium hydroxide solution until the pH is 6. The dyestuff is salted out with 10% sodium chloride and filtered off with suction.
The aminoazo dyestuff so obtained is dissolved in 300 ml of water at pH 7, 6.9 g sodium nitrite are then added, the mixture is cooled, and 28 ml of concentrated hydrochloric acid are added at 0.degree.- 5.degree. C. After diazotising for one hour, the disazo suspension is poured into a solution of 19.3 g (0.1 mol) 2-phenyl-indole in glacial acetic acid and somewhat buffered with sodium acetate or solution of sodium hydroxide. After coupling, the dyestuff is isolated in the usual way and dried at 90.degree. C. The dyestuff dyes polyamide from a weakly acidic or neutral bath in reddish-orange shades of good fastness to light.
When the procedure described above is followed, but with the use of the compounds mentioned in Column I as diazo components, those of Column II as middle components and those of Column III as final components, then valuable disazo water-soluble dyestuffs are again obtained, which dye polyamide in orange to bluish red shades of good fastness to light and good neutral affinity.
__________________________________________________________________________No. I II III__________________________________________________________________________56 ##STR103## ##STR104## ##STR105##57 " " ##STR106##58 " " ##STR107##59 " ##STR108## ##STR109##60 " " ##STR110##61 " " ##STR111##62 " " ##STR112##63 " ##STR113## ##STR114##64 " ##STR115## ##STR116##65 " " ##STR117##66 ##STR118## ##STR119## ##STR120##67 " " ##STR121##68 " " ##STR122##69 " ##STR123## ##STR124##70 " " ##STR125##71 " " ##STR126##72 " ##STR127## ##STR128##73 " " ##STR129##74 " ##STR130## ##STR131##75 " " ##STR132##76 " " ##STR133##77 " ##STR134## ##STR135##78 " " ##STR136##79 ##STR137## ##STR138## ##STR139##80 " " ##STR140##81 " " ##STR141##82 " " ##STR142##83 " ##STR143## ##STR144##84 " " ##STR145##85 " " ##STR146##86 " " ##STR147##87 " ##STR148## ##STR149##88 " ##STR150## ##STR151##89 " " ##STR152##90 " " ##STR153##91 " ##STR154## ##STR155##92 " " ##STR156##93 " ##STR157## ##STR158##94 " " ##STR159##95 " " ##STR160##96 ##STR161## ##STR162## ##STR163##97 ##STR164## ##STR165## ##STR166##98 " " ##STR167##99 " " ##STR168##100 " " ##STR169##101 " ##STR170## ##STR171##102 " " ##STR172##103 " " ##STR173##104 " " ##STR174##__________________________________________________________________________
EXAMPLE 105
0.1 mol 4-acetylamino-aniline are diazotised in the usual way and the product is combined in an alkaline medium with a solution of 0.1 mol phenol-3-sulphonic acid. When the coupling is completed, the resultant monoazo dyestuff is isolated and methylated in the usual way with dimethyl sulphate. The methoxy dyestuff is hydrolysed with a 4% aqueous sodium hydroxide solution for about one hour. The resultant aminoazo compound is diazotised at room temperature and the product is combined with a solution of 0.1 mol 2-phenylindole in glacial acetic acid. The product is isolated in the usual way and after drying and grinding, there is obtained a dyestuff which dyes polyamide from a neutral or weakly acidic bath in reddish orange shades.

Claims

1. Disazo dyestuff which in the form of the free acid corresponds to the formula ##STR175## in which R.sub.1 stands for hydrogen, alkyl of 1-4 carbon atoms, or phenyl;
R.sub.2, r.sub.3 and R.sub.4, independently of one another, stand for hydrogen, chloro, bromo, alkyl of 1-4 carbon atoms, alkoxy of 1-4 carbon atoms, alkylcarbonylamino of 1-4 carbon atoms, methylsulfonylamino, phenylcarbonylamino, chlorophenyl carbonylamino, or phenylsulfonylamino;
R.sub.5 stands for hydrogen, alkyl of 1-4 carbon atoms or alkoxy of 1-4 carbon atoms;
R.sub.6 and R.sub.7 independently of one another, stand for hydrogen, hydroxy, cyano, chloro, bromo, alkylcarbonyloxy of 1-4 carbon atoms in the alkyl portion, alkoxycarbonyloxy of 1-4 carbon atoms in the alkoxy portion alkoxy carbonyl of 1-4 carbon atoms in the alkoxy portion, or phenyl; and
X stands for alkylene of 1-4 carbon atoms.
2. Disazo dyestuff which in the form of the free acid corresponds to the formula ##STR176## in which R.sub.1 ' stands for alkyl with 1 - 4 carbon atoms;
R.sub.2 ' stands for hydrogen or alkoxy with 1 - 4 carbon atoms;
R.sub.3 ' stands for hydrogen or alkyl with 1 - 4 carbon atoms;
R.sub.4 ' stands for hydrogen, alkyl with 1 - 4 carbon atoms, Cl, Br or an alkyl-carbonylamino group with 1 - 4 carbon atoms;
R.sub.5 ' stands for hydrogen or alkoxy with 1 - 4 carbon atoms;
X stands for --CH.sub.2 --CH.sub.2 -- or --CH.sub.2 --, and
R.sub.6 ' and R.sub.7 ', independently of one another, stand for hydrogen Cl, OH, CN, alkyl-carbonyloxy with 1 - 4 carbon atoms in the alkyl group, alkoxycarbonyloxy with 1 - 4 carbon atoms in the alkoxy group or alkoxy-carbonyl with 1 - 4 carbon atoms in the alkoxy group.
3. The dyestuff which in the form of the free acid corresponds to the formula ##STR177##
4. The dyestuff which in the form of the free acid corresponds to the formula ##STR178##
5. The dyestuff which in the form of the free acid corresponds to the formula ##STR179##

Priority Claims (2)

Number	Date	Country	Kind
2006733	Feb 1970	DT
2049810	Oct 1970	DT

US Referenced Citations (5)

Number	Name	Date
1835393	Hentrich et al.	Dec 1931
3070592	Baumann et al.	Dec 1962
3479332	Jirou et al.	Nov 1969
3485814	Speck	Dec 1969
3557080	Dehnert et al.	Jan 1971

Foreign Referenced Citations (1)

Number	Date	Country
952,061	Mar 1964	UK

Sulfaphenyl-azo-phenyl-azo-aminophenyl dyestuffs

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