Navy dye mixtures

Abstract

Navy dye mixtures essentially contain dyes of the formula I ##STR1## where X is hydrogen, chlorine or bromine, the radicals R.sup.1 independently of one another are each methyl or ethyl and R is a radical of the formula ##STR2## where A is ##STR3## B is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, phenyl-C.sub.1 -C.sub.4 -alkyl, phenoxy-C.sub.2 - or -C.sub.3 -alkyl or cyclohexyl and R.sup.2 is C.sub.1 -C.sub.4 -alkyl, the mixtures containing from 20 to 80 parts of dyes in which R is NH-A-COOB and from 80 to 20 parts of dyes in which R is ##STR4## The novel mixtures are very useful for dyeing synthetic polyesters, and give dyeings which have, in particular, very good heatfastness.

Description

The present invention relates to navy dye mixtures which essentially contain dyes of the formula I ##STR5## where X is hydrogen, chlorine or bromine, the radicals R.sup.1 independently of one another are each methyl or ethyl and R is a radical of the formula ##STR6## where A is ##STR7## B is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, phenyl- C.sub.1 -C.sub.4 -alkyl, phenoxy-C.sub.2 - or -C.sub.3 -alkyl or cyclohexyl and R.sup.2 is C.sub.1 -C.sub.4 -alkyl, the mixtures containing from 20 to 80 parts of dyes in which R is NH-A-COOB and from 80 to 20 parts of dyes in which R is ##STR8##

Specific examples of radicals B are CH.sub.3, C.sub.2 H.sub.5, n- and i--C.sub.3 H.sub.7, n- and i--C.sub.4 H.sub.9, C.sub.2 H.sub.4 OH, C.sub.2 H.sub.4 OCH.sub.3, C.sub.2 H.sub.4 OC.sub.2 H.sub.5, C.sub.2 H.sub.4 OC.sub.3 H.sub.7, C.sub.2 H.sub.4 OC.sub.4 H.sub.9, C.sub.2 H.sub.4 CN, C.sub.3 H.sub.6 OH, C.sub.3 H.sub.6 OCH.sub.3, C.sub.3 H.sub.G OC.sub.2 H.sub.5, C.sub.3 H.sub.6 OC.sub.3 H.sub.7, C.sub.3 H.sub.6 OC.sub.4 H.sub.9, ##STR9## CH.sub.2 C.sub.6 H.sub.5, CH.sub.2 C.sub.6 H.sub.4 CH.sub.3, CH.sub.2 C.sub.6 H.sub.4 Cl, CH.sub.2 C.sub.6 H.sub.4 OCH.sub.3, C.sub.2 H.sub.4 C.sub.6 H.sub.5, C.sub.2 H.sub.4 C.sub.6 H.sub.4 CH.sub.3, C.sub.3 H.sub.6 C.sub.6 H.sub.5, C.sub.4 H.sub.9 C.sub.6 H.sub.5, CH-C.sub.6 H.sub.5, C.sub.2 H.sub.4 OC.sub.6 H.sub.5, C.sub.3 H.sub.6 OC.sub.6 H.sub.5, C.sub.2 H.sub.4 OC.sub.6 H.sub.4 CH.sub.3, C.sub.2 H.sub.4 OC.sub.6 H.sub.3 (CH.sub.3).sub.2, and C.sub.2 H.sub.4 OC.sub.6 H.sub.4 Cl, the radicals C.sub.3 H.sub.6 and C.sub.4 H.sub.8 including the n- and isoalkylene groups.

A is, in particular, --C.sub.2 H.sub.4 --. X is preferably bromine, R.sup.1 is preferably methyl or ethyl, R.sup.2 is preferably methyl and B is preferably benzyl, phenylethyl or phenoxyethyl.

Preferred mixtures contain from 40 to 60 parts of dyes in which R is NHC.sub.2 H.sub.4 COOB and from 60 to 40 parts of dyes in which R is ##STR10##

The mixtures can be prepared by mixing the individual components, or synthetically, for example by means of a mixed coupling. The dye mixtures can also contain small amounts of other dyes, e.g. compounds of the formula I where R is NHC.sub.2 H.sub.4 CN, NHCH.sub.2--CH.dbd.CH.sub.2 or N(CH.sub.2 CH.dbd.CH.sub.2).sub.2, resulting from the synthesis of the coupling components.

On synthetic polyesters, the novel mixtures give navy dyeings which have excellent heatfastness and good wetfastness, lightfastness and fastness to post-setting. Furthermore, they display temperature-independent exhaustion properties, good build up and a resistance to reducing substances.

In the Examples which follow, parts and percentages are by weight, unless stated otherwise. ##STR11##

EXAMPLE 1

60 parts of the dye in which X is bromine, R.sup.1 is methyl and R is ##STR12## and 40 parts of the dye in which X is bromine, R.sup.1 is methyl and R is ##STR13## were mixed thoroughly in a ball mill to give 100 parts of a dye mixture according to the invention.

EXAMPLE 2

40 parts of the dye in which X is bromine, R.sup.1 is methyl and R is ##STR14## and 60 parts of the dye in which X is bromine, R.sup.1 is methyl and R is ##STR15## were combined in a ball mill to give 100 parts of a dye mixture according to the invention.

EXAMPLE 3

50 parts of the dye in which X is bromine, R.sup.1 is methyl and R is ##STR16## 25 parts of the dye in which X is bromine, R.sup.1 is methyl and R is ##STR17## and 25 parts of the dye in which X is bromine, R.sup.1 is methyl and R is ##STR18## were mixed in a ball mill to give 100 parts of a dye mixture according to the invention.

EXAMPLE 4

26.2 parts of 2-bromo-4,6-dinitroaniline were dissolved in 100 parts of 96% strength sulfuric acid, diazotization was carried out at 5.degree.-10.degree. C. with 32 parts of nitrosylsulfuric acid (11.5% of N.sub.2 O.sub.3) and the mixture was stirred for a further 16 hours at 10.degree.-15.degree. C. 20.5 parts of 3-(N-.beta.-benzyloxycarbonylethylamino)-4-methoxyacetanilide and 10.9 parts of 3-(N-allyl-N-.beta.-cyanoethylamino)-4-methoxyacetanilide were dissolved in 250 parts of dimethylformamide, the solution was stirred into a mixture of 60 parts of 32% strength hydrochloric acid and 30 parts of water, and 400 parts of ice were added. The diazonium salt solution was then run in at 0.degree.-5.degree. C. When coupling was complete, the suspension was heated at 40.degree. C., the dye was filtered off, washed neutral with water and dried to give 55 parts of a novel dye mixture containing about 35 parts of the dye in which X is bromine, R.sup.1 is methyl and R is ##STR19## and about 20 parts of the dye in which X is bromine, R.sup.1 is methyl and R is ##STR20##

EXAMPLE 5 (HT PROCESS)

100 parts of a polyester yarn were treated in a dyeing bath which contained 1000 parts of water, 2.5 parts of the finely divided dye mixture prepared as described in Example 1 and 1.5 parts of a product obtained by an addition reaction of 50 moles of ethylene oxide with 1 mole of sperm oil alcohol followed by sulfonation of the product. The dyeing was started at 60.degree. C., the temperature was then increased to 125.degree. C. in the course of 20 minutes, and dyeing was continued at this temperature for a further 90 minutes.

The resulting deep navy dyeing had good lightfastness and fastness to thermosetting and very good wet fastness.

EXAMPLE 6 (THERMOSOL PROCESS)

Using a three-roll padding mangle, a polyester fabric was impregnated with a dyeing liquor which contained, per 1000 parts, 45 parts of the finely divided dye mixture prepared as described in Example 2, 15 parts of a 20% strength aqueous solution of a copolymer of acrylic acid with acrylamide and 940 parts of water.

After the impregnation with 65% wet pickup, the fabric was dried at 120.degree. C. and then thermosoled for 1 minute at 220.degree. C. The resulting deep navy dyeing had excellent fastness properties.

EXAMPLE 7 (TEXTILE PRINTING)

A polyester fabric was printed with a paste which contained, per 1000 parts, 50 parts of the finely divided dye mixture prepared as described in Example 3, 20 parts of a reaction product obtained from 1 mole of castor oil and 40 moles of ethylene oxide, 600 parts of a crystal gum thickening, 10 parts of triisobutyl phosphate and 320 parts of water.

After drying, the printed fabric was steam-treated for 15 minutes under 2.5 bar. The resulting deep navy print had excellent fastness properties.

Claims

1. A navy dye mixture which essentially contains dyes of the formula I ##STR21## where X is hydrogen, chlorine or bromine, the radicals R.sup.1 independently of one another are each methyl or ethyl and R is a radical of the formula ##STR22## where A is--C.sub.2 H.sub.4 --, ##STR23## B is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, phenyl-C.sub.1 -C.sub.4 -alkyl, phenoxy-C.sub.2 - or -C.sub.3 -alkyl or cyclohexyl and R.sup.2 is C.sub.1 -C.sub.4 -alkyl, the mixtures containing from 20 to 80 parts of dyes in which R is NH-A-COOB and from 80 to 20 parts of dyes in which R is ##STR24##

2. A mixture as claimed in claim 1, wherein X is bromine, R.sup.2 is methyl and B is benzyl, phenylethyl or phenoxyethyl.

3. A mixture as claimed in claim 1, which contains from 40 to 60 parts of dyes in which R is NHC.sub.2 H.sub.4 COOB and from 60 to 40 parts of dyes in which R is ##STR25## and/or N(C.sub.2 H.sub.4 OCOR.sup.2).sub.2.