Phenylazophenyl dyes having an alkoxyacylamino group on the coupling component radical

Description

This invention relates to compounds of Formula I which are highly suitable for use as disperse dyes. As such they are employed for dyeing high molecular weight synthetic and regenerated organic fibers, either in loose form, as yarn or in the various textile forms. The dyes are of high tinctorial strength, have good affinity, are resistant to sublimation, and give dyeings of notably good light and wet fastness.
These new dyes have the formula ##STR2## wherein R.sub.1 is chloro, bromo, cyano, nitro, alkylsulfonyl, substituted alkylsulfonyl, phenylsulfonyl or substituted phenylsulfonyl.
R.sub.2 is hydrogen, chloro or bromo,
R.sub.3 is hydrogen, chloro, bromo or acylamino, with the proviso that at least one of R.sub.2 and R.sub.3 is hydrogen,
R.sub.4 is hydrogen, alkyl, substituted alkyl, alkoxy or substituted alkoxy,
each of R.sub.5 and R.sub.6 is independently alkyl or substituted alkyl, wherein each substituent of substituted alkyl is independently chloro, bromo, cyano, hydroxy, alkoxy, chloroalkoxy, bromoalkoxy, cyanoalkoxy, formyloxy, alkylcarbonyloxy, substituted alkylcarbonyloxy, benzoyloxy, substituted benzoyloxy, alkoxycarbonyl, substituted alkoxycarbonyl, phenoxycarbonyl, substituted phenoxycarbonyl, alkoxycarbonyloxy, substituted alkoxycarbonyloxy, phenoxycarbonyloxy or substituted phenoxycarbonyloxy,
R.sub.7 is alkyl or substituted alkyl,
X is --CO--, --CO.sub.2 -- or --SO.sub.2 --, and
n is 2, 3 or 4.
Each alkyl and alkoxy radical, including the alkyl chain of substituted alkyl, the alkoxy chain of substituted alkoxy, the alkyl radical of alkylcarbonyloxy, the alkoxy radical of alkoxycarbonyl, etc., contains 1 to 4 carbon atoms. The substituents of substituted alkyl and substituted alkoxy, except as otherwise defined, are halo, notably chloro and bromo, hydroxy, cyano and alkoxy. The substituents of the substituted phenyl radicals, including substituted benzoyloxy, phenoxycarbonyl, etc., are chloro, bromo, cyano, nitro, acyl, alkyl and alkoxy.
The preferred acyl groups are R--Y-- and R'--Z--,
wherein
R is a hydrocarbyl radical which may contain the above-mentioned substituents and/or hetero atoms, preferably an alkyl or phenyl radical,
y is --O--CO-- or --SO.sub.2 --,
R' is hydrogen or R, and
Z is --CO--, --NR'--CO-- or --NR'--SO.sub.2 --.
Compounds of Formula I
wherein
R.sub.1 is chloro, bromo, cyano, nitro, unsubstituted or substituted alkylsulfonyl or phenylsulfonyl,
R.sub.2 is hydrogen, chloro or bromo,
R.sub.3 is hydrogen, chloro, bromo or acylamino, with the proviso that at least one of R.sub.2 and R.sub.3 is hydrogen,
R.sub.4 is hydrogen or unsubstituted or substituted alkyl or alkoxy,
each of R.sub.5 and R.sub.6 is independently alkyl or alkyl substituted by chloro, bromo, cyano, hydroxy, alkoxy, chloroalkoxy, bromoalkoxy, cyanoalkoxy, unsubstituted or substituted alkylcarbonyloxy, benzoyloxy, alkoxycarbonyl, phenoxycarbonyl, alkoxycarbonyloxy or phenoxycarbonyloxy,
R.sub.7 is alkyl or substituted alkyl,
X is --CO--, , --CO.sub.2 -- or --SO.sub.2 --, and
n is 2, 3 or 4,
wherein each alkyl and alkoxy radical has 1 to 4 carbon atoms,
each substituent of a substituted alkyl or alkoxy radical is halo (notably chloro or bromo), hydroxy or cyano,
each substituent of a substituted phenyl group (including the phenyl nucleus of benzoyl, phenoxycarbonyl, etc. radicals) is chloro, bromo, cyano, nitro, acyl, alkyl or alkoxy, and each acyl radical is as defined above, are of interest.
The compounds of Formula I are produced by diazotizing an aniline of the formula ##STR3## and coupling the resulting diazonium compound with a compound of the formula
The compounds of Formula I which have the specific formula ##STR4## wherein R.sub.8 is alkylcarbonyl, alkoxycarbonyl, benzoyl or phenoxycarbonyl, and
R.sub.9 is cyano, alkoxycarbonyl, phenoxycarbonyl, alkylcarbonyloxy, alkoxycarbonyloxy, benzoyloxy or phenoxycarbonyloxy,
can be produced by acylation of an azo compound of the formula ##STR5## wherein R.sub.10 is alkoxycarbonyl, phenoxycarbonyl, cyano or hydroxy, with an acid of the formula
R.sub.8 -- OH (VI),
wherein R.sub.8 is alkylcarbonyl, alkoxycarbonyl, benzoyl or phenoxycarbonyl, or with a functional derivative of such an acid. Suitable functional derivatives are, for example, the anhydrides and halides, in particular the chlorides of these acids.
The diazotizing and coupling reactions are carried out in accordance with the standard methods that have been known for over a century.
The coupling components of Formula III are produced by known methods, e.g., by reaction of an amine of the formula ##STR6## with an acid of the formula HOOC(CH.sub.2).sub.n --O--R.sub.7 at a temperature in the range of about 150.degree. C. to 200.degree. C. with cleavage of water, followed by reduction of the nitro group and introduction of the radicals R.sub.5 and R.sub.6 either by condensation or addition.
Preferred compounds of Formula I have the formula ##STR7## wherein R.sub.2 is hydrogen, chloro or bromo,
R.sub.11 is chloro, bromo, cyano, nitro, methylsulfonyl, phenylsulfonyl or tolylsulfonyl,
R.sub.13 is hydrogen, chloro, bromo, alkylcarbonylamino or substituted alkylcarbonylamino, wherein the alkyl radical of alkylcarbonylamino and substituted alkylcarbonylamino has 1 or 2 carbon atoms and the substituents of substituted alkylcarbonylamino are chloro or bromo, with the proviso that at least one of R.sub.2 and R.sub.13 is hydrogen,
R.sub.14 is hydrogen, methoxy or ethoxy, each of R.sub.15 and R.sub.16 is independently alkyl of 1 to 4 carbon atoms or alkyl of 1 to 4 carbon atoms substituted by hydroxy, cyano, methoxy, ethoxy, acetoxy, propionyloxy, butyryloxy, benzoyloxy, methoxycarbonyl, ethoxycarbonyl, methoxycarbonyloxy or ethoxycarbonyloxy,
R.sub.17 is methyl, ethyl or propyl, and m is 2 or 3,
and especially those compounds of Formula VII wherein
R.sub.11 is cyano,
R.sub.13 is hydrogen,
R.sub.14 is hydrogen,
R.sub.15 is ethyl,
R.sub.16 is ethyl, and
R.sub.2, r.sub.17 and m are as defined above.
Also of interest are those compounds of Formula VII
wherein
R.sub.11 is cyano, nitro, phenylsulfonyl or tolylsulfonyl,
R.sub.13 is hydrogen, alkylcarbonylamino or monosubstituted alkylcarbonylamino, wherein the alkyl radical of alkylcarbonylamino and monosubstituted alkylcarbonylamino has 1 or 2 carbon atoms and the substituent of monosubstituted alkylcarbonylamino is chloro or bromo, with the proviso that at least one of R.sub.2 and R.sub.13 is hydrogen.
each of R.sub.15 and R.sub.16 is independently alkyl of 1 to 4 carbon atoms or alkyl of 1 to 4 carbon atoms substituted by hydroxy, cyano, acetoxy, propionyloxy, methoxycarbonyl, ethoxycarbonyl, methoxycarbonyloxy or ethoxycarbonyloxy, and
R.sub.2, r.sub.14, r.sub.17 and m are as defined following Formula VII, as well as those compounds of Formula VII
wherein
R.sub.11 is cyano, nitro, phenylsulfonyl or p-tolylsulfonyl,
R.sub.13 is hydrogen, acetamido, .beta.-chloropropionamido or .beta.-bromopropionamido, with the proviso that at least one of R.sub.2 and R.sub.13 is hydrogen,
each of R.sub.15 and R.sub.16 is independently methyl, ethyl, propyl, butyl, .beta.-hydroxyethyl, .beta.-cyanoethyl, .beta.-acetoxyethyl, .beta.-propionyloxyethyl, .beta.-methoxycarbonyloxyethyl, .beta.-ethoxycarbonyloxyethyl, .beta.-methoxycarbonylethyl or .beta.-ethoxycarbonylethyl, and
R.sub.2, r.sub.14, r.sub.17 and m are as defined following Formula VII.
Also preferred are the compounds of the formula ##STR8## wherein R.sub.1 is nitro, cyano, phenylsulfonyl or tolylsulfonyl,
R.sub.2 is hydrogen, chloro or bromo,
R.sub.13 is hydrogen, formamido, acetamido, propionamido, chloropropionamido or bromopropionamido, with the proviso that at least one of R.sub.2 and R.sub.13 is hydrogen,
R.sub.14 is hydrogen, methoxy or ethoxy,
R.sub.25 is alkyl, cyanoalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.26 is alkyl, hydroxyalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.27 is alkoxyalkyl,
X is --CO--, --CO.sub.2 -- or --SO.sub.2 --, and
m is 2 or 3,
wherein each alkyl, hydroxyalkyl and alkyl and alkoxy radical of each cyanoalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl, alkoxycarbonylalkyl and alkoxyalkyl independently has 1 to 4 carbon atoms.
Particularly preferred are compounds of the formula ##STR9## wherein R.sub.2 is hydrogen, chloro or bromo,
R.sub.14 is hydrogen, methoxy or ethoxy,
R.sub.21 is cyano, phenylsulfonyl or tolylsulfonyl,
R.sub.25 is alkyl, cyanoalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.26 is alkyl, hydroxyalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.27 is alkyl or monosubstituted alkyl wherein the substituent of monosubstituted alkyl is alkoxy, chloro, bromo or cyano,
X is --CO--, --CO.sub.2 -- or --SO.sub.2 --, and
m is 2 or 3.
wherein each alkyl and alkoxy radical, including each alkyl and alkoxy radical of hydroxyalkyl, cyanoalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl, alkoxycarbonylalkyl and monosubstituted alkyl, independently has 1, 2, 3 or 4 carbon atoms and may be straight or branched.
Compounds of Formula VIII
wherein
R.sub.21 is cyano or phenylsulfonyl,
R.sub.25 is methyl, ethyl, .beta.-formyloxyethyl, .beta.-cyanoethyl, .beta.-acetoxyethyl, .beta.-methoxycarbonyloxyethyl, .beta.-ethoxycarbonyloxyethyl, .beta.-methoxycarbonylethyl or .beta.-ethoxycarbonylethyl,
R.sub.26 is ethyl, .beta.-hydroxyethyl, .beta.-formyloxyethyl, .beta.-acetoxyethyl, .beta.-methoxycarbonyloxyethyl, .beta.-ethoxycarbonyloxyethyl, .beta.-methoxycarbonylethyl or .beta.-ethoxycarbonylethyl,
R.sub.27 is methyl or ethyl,
m is 2, and
R.sub.2, r.sub.14 and X are as defined above are particularly preferred.
Also preferred are those compounds of Formula VIII
wherein
R.sub.25 is alkyl, cyanoalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.26 is alkyl, hydroxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.27 is alkyl or monosubstituted alkyl wherein the substituent is chloro, bromo or cyano, and
R.sub.2, r.sub.14, r.sub.21, x and m are as defined following Formula VIII.
Also particularly preferred are those compounds of Formula VIII
wherein
R.sub.14 is hydrogen or ethoxy.
R.sub.25 is ethyl, .beta.-cyanoethyl or .beta.-acetoxyethyl,
R.sub.26 is ethyl or .beta.-acetoxyethyl,
R.sub.27 is methyl, ethyl or propyl,
X is --CO--,
m is 2, and
R.sub.2 and R.sub.21 are as defined following Formula VIII.
Also of interest are those compounds of Formula VIII
wherein
R.sub.27 is alkoxyalkyl (especially .beta.-alkoxyethyl), and
R.sub.2, r.sub.14, r.sub.21, r.sub.25, r.sub.26, x and m are as defined following Formula VIII, and of particular interest are those compounds of Formula VIII
wherein
R.sub.14 is hydrogen,
R.sub.21 is cyano,
R.sub.27 is .beta.-alkoxyethyl,
X is --CO--,
m is 2, and
R.sub.2, r.sub.25 and R.sub.26 are as defined following Formula VIII and particularly the compounds of this group wherein each of R.sub.25 and R.sub.26 is independently ethyl or .beta.-acetoxyethyl.
Also of interest are the compounds of Formula VIII wherein at least one of R.sub.25 and R.sub.26 is formyloxyalkyl, and R.sub.2, R.sub.14, R.sub.21, the other of R.sub.25 and R.sub.26 if both are not formyloxyalkyl, R.sub.27, X and m are as defined following Formula VIII and particularly those compounds of this group wherein R.sub.25 and R.sub.26 are .beta.-formyloxyethyl.
Compounds of Formula VIII
wherein
R.sub.27 is chloroalkyl, bromoalkyl or cyanoalkyl, and
R.sub.2, r.sub.14, r.sub.21, r.sub.25, r.sub.26, x and m are as defined following Formula VIII are also of interest.
Also particularly preferred are compounds of the formula ##STR10## wherein R.sub.2 is hydrogen, chloro or bromo,
R.sub.13 is hydrogen, formamido, acetamido, propionamido, chloropropionamido or bromopropionamido, with the proviso that at least one of R.sub.2 and R.sub.13 is hydrogen,
R.sub.14 is hydrogen, methoxy or ethoxy,
R.sub.25 is alkyl, cyanoalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.26 is alkyl, hydroxyalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.27 is alkyl or monosubstituted alkyl wherein the substituent of monosubstituted alkyl is alkoxy, chloro, bromo or cyano,
X is --CO--, --CO.sub.2 -- or --SO.sub.2 --, and
m is 2 or 3,
wherein each alkyl and alkoxy radical, including each alkyl and alkoxy radical of hydroxyalkyl, cyanoalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl, alkoxycarbonylalkyl and monosubstituted alkyl, independently has 1, 2, 3, or 4 carbon atoms and may be straight or branched.
Compounds of Formula IX
wherein
R.sub.13 is hydrogen or acetamido, with the proviso that at least one of R.sub.2 and R.sub.13 is hydrogen,
R.sub.25 is methyl, ethyl, .beta.-cyanoethyl, .beta.-formyloxyethyl, .beta.-acetoxyethyl, .beta.-methoxycarbonylethyl, .beta.-ethoxycarbonylethyl, .beta.-methoxycarbonyloxyethyl or .beta.-ethoxycarbonyloxyethyl,
R.sub.26 is ethyl, .beta.-hydroxyethyl, .beta.-formyloxyethyl, .beta.-acetoxyethyl, .beta.-methoxycarbonyloxyethyl, .beta.-ethoxycarbonyloxyethyl, .beta.-methoxycarbonylethyl or .beta.-ethoxycarbonylethyl,
R.sub.27 is methyl, ethyl or propyl,
m is 2, and
R.sub.2, r.sub.14 and X are as defined above are particularly preferred.
Also preferred are the compounds of Formula IX
wherein
R.sub.13 is hydrogen, acetamido, chloropropionamido or bromopropionamido, with the proviso that at least one of R.sub.2 and R.sub.13 is hydrogen,
R.sub.25 is alkyl, cyanoalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.26 is alkyl, hydroxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.27 is alkyl or monosubstituted alkyl wherein the substituent is chloro, bromo or cyano, and
R.sub.2, r.sub.14, x and m are as defined following Formula IX are particularly preferred.
Also particularly preferred are those compounds of Formula IX
wherein
R.sub.13 is hydrogen, acetamido, chloropropionamido or bromoprepionamido, with the proviso that at least one of R.sub.2 and R.sub.13 is hydrogen,
R.sub.25 is ethyl, butyl, .beta.-cyanoethyl, .beta.-propionyloxyethyl, .beta.-methoxycarbonylethyl, .beta.-ethoxycarbonylethyl or .beta.-ethoxycarbonyloxyethyl,
R.sub.26 is methyl, ethyl, propyl, .beta.-hydroxyethyl, .beta.-propionyloxyethyl, .beta.-ethoxycarbonylethyl, .beta.-methoxycarbonyloxyethyl or .beta.-ethoxycarbonyloxyethyl,
R.sub.27 is methyl or ethyl, and
R.sub.2, r.sub.14, x and m are as defined following Formula IX.
Also of interest are those compounds of Formula IX
wherein
R.sub.27 is alkoxyalkyl (especially .beta.-alkoxyethyl), and
R.sub.2, r.sub.13, r.sub.14, r.sub.25, r.sub.26, x and m are as defined following Formula IX. and of particular interest are those compounds of Formula IX
wherein
R.sub.13 is hydrogen,
R.sub.14 is ethoxy,
R.sub.25 is ethyl or .beta.-acetoxyethyl,
R.sub.26 is ethyl or .beta.-acetoxyethyl,
R.sub.27 is .beta.-alkoxyethyl,
X is --CO-- or --CO.sub.2 --,
m is 2, and
R.sub.2 is as defined following Formula IX.
Also of interest are the compounds of Formula IX
wherein
at least one of R.sub.25 and R.sub.26 is formyloxyalkyl, and
R.sub.2, r.sub.13, r.sub.14, the other of R.sub.25 and R.sub.26 if both aren't formyloxyalkyl, R.sub.27, X and m are as defined following Formula IX and particularly those compounds of this group wherein R.sub.25 and R.sub.26 are .beta.-formyloxyethyl as well as compounds of Formula IX
wherein
R.sub.27 is chloroalkyl, bromoalkyl or cyanoalkyl, and
R.sub.2, r.sub.13, r.sub.14, r.sub.25, r.sub.26, x and m are as defined following Formula IX.
The new compounds of formula I are worked up as dyeing preparations by known methods, for example by grinding in the presence of dispersing agents and/or fillers. The ground mixtures are vacuum or injection dried if dry preparations are desired. The preparations are added to a suitable volume of water for exhaust dyeing, pad dyeing and printing at long or short liquor ratio.
From aqueous dispersion the dyes build up powerfully on synthetic and regenerated organic fibres, both in the loose form and as yarn or textiles. They are especially suitable for dyeing and printing polyester, cellulose acetate, cellulose triacetate and polyamide fibres and textiles, and can also be applied to polyolefin fibres. The known dyeing and printing methods are used, for instance the process described in French Pat. No. 1,445,371.
The dyeings obtained have good fastness in a comprehensive range of properties, the fastness to light and to thermofixation, sublimation and pleating being notably good. They are very fast to wet treatments such as washing, water, sea water, perspiration, solvents, especially dry cleaning liquor, lubricants, and to rubbing, cross dyeing, ozone, gas fumes and chlorine. The dyeings are stable to pre-cure and post-cure permanent press finishing and to soil release finishes. They show good stability to reducing action in the dyeing of textiles containing wool and reserve wool and cotton. The dyeings are dischargeable.
This invention therefore serves the purpose, inter alia, of supplying the textile industry with new, superior dyes for dyeing the synthetic fibre and regenerated fibre textiles which are being produced on an ever growing scale, and with which a prime consideration is to have dyes which are applicable by the rationalized continuous and high-temperature dyeing processes in use today.
In the following Examples the parts are by weight and the temperatures in degrees centigrade.

EXAMPLE 1
At a temperature near to 70.degree. 7 parts of sodium nitrite are added to 155 parts of concentrated sulfuric acid, followed at 15.degree. by 26.2 parts 2-bromo-4,6-dinitroamino-benzene. The solution is stirred for 2 hours at 15.degree.-20.degree. and the diazonium salt solution thus formed is cooled to about 0.degree. and, at this temperature, combined with a solution of 5 parts of urea and 29.4 parts 1-methoxypropionylamino-3-N,N-diethylamino-4-ethoxybenzene in 100 parts of glacial acetic acid. The coupling reaction is brought to a close by addition of concentrated sodium acetate solution until the pH of the reaction mixture is about 4. The dye settles out and is filtered, washed with water until free of acid, and dried.
Applied to polyester fibres or textiles, the thus obtained dye of the formula ##STR11## gives brilliant greenish blue shades of great depth which have very good fastness properties.
EXAMPLE 2
At a temperature not higher than 70.degree. 7 parts of sodium nitrite are added to 155 parts of concentrated sulphuric acid, followed at 15.degree. by 24.2 parts of 2-amino-3-bromo-5-nitrobenzonitrile. The solution is stirred for 2 hours at 15.degree.-20.degree. and the diazonium salt solution thus formed is combined with a solution of 2 parts of urea and 25 parts of 1-N,N-diethylamino-3-(3'-methoxypropionyl)-anilide in 100 parts of glacial acetic acid. After the addition of 500 parts of ice-water the reaction solution is stirred for a further 2 hours, on which the dye settles out. It is filtered, washed with water until free of acid, and dried.
Applied to polyester fibres or textiles, this dye gives brilliant blue shades of great depth which have very good fastness properties.
Further dyes of Formula I which can be produced by analogy with the foregoing Examples are specified in the table below.
TABLE Shade on Ex. polyester No. R.sub.1 R.sub.2 R.sub.3 R.sub.4 R.sub.5 R.sub.6 R.sub.7 n X fiber 3 Cl H H H CH.sub.2 CH.sub.2 OCOCH.sub.3 CH.sub.2 CH.sub.2 OCOCH.sub.3 CH.sub.3 2 CO blue 4 CN H H H " " C.sub.2 H.sub.5 2 " rubine 5 CN H H H CH.sub.2 CH.sub.2 CN " " 2 " " 6 SO.sub.2 CH.sub.3 H H H " " CH.sub.3 2 " red 7 NO.sub.2 Br H H C.sub.2 H.sub.5 C.sub.2 H.sub.5 " 2 " violet 8 " " H OC.sub.2 H.sub.5 CH.sub.2 CH.sub. 2 CN CH.sub.2 CH.sub.2 OH " 2 " blue 9 " " H " CH.sub.2 CH.sub.2 OCOC.sub.2 H.sub.5 CH.sub.2 CH.sub.2 OCOC.sub.2 H.sub.5 " 2 " " 10 " " H " " " " 3 " reddish blue 11 " Cl H " CH.sub.2 CH.sub.2 CN CH.sub.2 CH.sub.2 OCH.sub.3 " 2 " blue 12 " H Cl H C.sub.2 H.sub.5 C.sub.2 H.sub.5 " 2 " " 13 " H NHCOCH.sub.3 H " " " 2 " reddish blue 14 " H ##STR12## H " " " 2 " " 15 CN Br H H C.sub.2 H.sub.5 C.sub.2 H.sub.5 CH(CH.sub.3).sub.2 2 CO blue 16 H.sub.5 C.sub.6SO.sub.2 Cl H OC.sub.2 H.sub. 5 CH.sub.2 CH.sub.2 OCOCH.sub.3 CH.sub.2 CH.sub.2 OCOCH.sub.3 CH.sub.3 2 " " 17 ##STR13## Cl H " " " " 2 " " 18 " Cl H " " " CH(CH.sub.3).sub.2 2 " " 19 " Cl H " " " C.sub.2 H.sub.5 2 " " 20 NO.sub.2 Br H OCH.sub.3 CH.sub.2 CH.sub.2 CN C.sub.2 H.sub.5 " 2 COO " 21 " Br H " " " " 2 SO.sub.2 " 22 " H ##STR14## H C.sub.2 H.sub.5 " " 2 CO reddish blue 23 " Br H OCH.sub.3 CH.sub.2 CH.sub.2 COOCH.sub.3 CH.sub.3 " 2 " " 24 " Cl H OC.sub.2 H.sub.5 CH.sub.2 CH.sub.2 COOC.sub.2 H.sub.5 C.sub.2 H.sub.5 " 2 " " 25 " Br H " C H.sub.2 CH.sub.2 OC.sub.2 H.sub.5 CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 " 2 " " 26 " Br H " CH.sub.2 CH.sub.2 CN CH.sub.2 CH.sub.2 CH.sub.3 " 2 " " 27 NO.sub.2 Br H OC.sub.2 H.sub.5 CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.3 CH.sub.2 CH.sub.2 COOC.sub.2 H.sub.5 C.sub.2 H.sub.5 2 CO reddish blue 28 " Br H " CH.sub.2 CH.sub.2 CN CH.sub.2 CH.sub.2 OCOOCH.sub.3 " 2 " " 29 " Br H " CH.sub.2 CH.sub.2 OCOOC.sub.2 H.sub.5 CH.sub.2 CH.sub.2 OCOOC.sub.2 H.sub.5 " 2 " " 30 " Br H " CH.sub.2 CH.sub.2 OCOC.sub.6 H.sub. 5 CH.sub.3 " 2 " " 31 CN H H H C.sub.2 H.sub.5 C.sub.2 H.sub.5 CH.sub.3 2 " red 32 H.sub.5 C.sub.6SO.sub.2 Br H OC.sub.2 H.sub.5 CH.sub.2 CH.sub.2 OCOCH.sub.3 CH.sub.2 CH.sub.2 OCOCH.sub.3 C.sub.2 H.sub.5 2 CO blue 33 CN H H H " " CH.sub.3 2 " bluish red 34 " H H H " " C H.sub.2 CH.sub.2 CH.sub.3 2 " " 35 " H H H " " CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.3 2 " " 36 " H H H " " CH.sub.2 CH.sub.2 OCH.sub.3 2 " " 37 " H H H " " CH.sub.2 CH.sub.2 OC.sub.2 H.sub.5 2 " " 38 " H H H " " CH.sub.2 CH.sub.2 OCH(CH.sub.3).sub.2 2 " " 39 " H H H " " CH.sub.2 CH.sub.2 OCH.sub.2 CH.sub.2 CH.sub.3 2 " " 40 " H H H " " CH.sub.3 2 " " 41 " H H H " " CH.sub.2 CH.sub.2 CH.sub.3 2 " " 42 CN H H H CH.sub.2 CH.sub.2 OCOCH.sub.3 CH.sub.2 CH.sub.2 OCOCH.sub.3 CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.3 2 CO bluish red 43 " H H H " " CH.sub.3 2 SO.sub.2 " 44 " H H H " " " 2 COO " 45 " H H H CH.sub.2 CH.sub.2 COOC.sub.2 H.sub.5 C H.sub.2 CH.sub.2 OH " 2 CO " 46 " H H H CH.sub.2 CH.sub.2 OCHO CH.sub.2 CH.sub.2 OCHO " 2 " " 47 " H H H CH.sub.2 CH.sub.2 OCOC.sub.2 H.sub.5 CH.sub.2 CH.sub.2 OCOC.sub.2 H.sub.5 " 2 " " 48 " H H H CH.sub.2 CH.sub.2 OCOOC.sub.2 H.sub.5 CH.sub.2 CH.sub.2 OCOOC.sub.2 H.sub.5 " 2 " " 49 " H H H CH.sub.2 CH.sub.2 OCOOCH.sub.3 CH.sub.2 CH.sub.2 OCOOCH.sub.3 " 2 " " 50 " H H H CH.sub.2 CH.sub.2 OCOCH.sub.2 CH.sub.2 CH.sub.3 " 2 " " CH.sub.2 CH.sub.2 OCOCH.sub.2 CH.sub.2 CH.sub.3 51 " H H H CH.sub.2 CH.sub.2 COOC.sub.2 H.sub.5 CH.sub.2 CH.sub.2 CH.sub.3 " 2 " " 52 CN Cl H H C.sub.2 H.sub.5 C.sub.2 H.sub.5 CH.sub.2 CH.sub.2 CH.sub.3 2 CO blue 53 " Cl H H " " CH.sub.2 CH.sub. 2 CH.sub.2 CH.sub.3 2 " " 54 " Br H H " " C.sub.2 H.sub.5 2 " " 55 " Br H H CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.3 CH.sub.2 CH.sub.2 COOC.sub.2 H.sub.5 " 2 " reddish blue 56 " Cl H H C.sub.2 H.sub.5 CH.sub.2 CH.sub.2 COOCH.sub.2 CH.sub.2 CH.sub.2 CH.sub.3 CH.sub.3 2 " " 57 " Br H H CH.sub.3 " " 2 " " 58 " H H H C.sub.2 H.sub.5 C.sub.2 H.sub.5 " 3 " violet 59 " H H H " " CH.sub.2 CH.sub.2 CN 2 " " 60 " H H H " " CH.sub.2 CH.sub.2 Cl 2 " " 61 " H H H " " CH.sub.2 CH.sub.2 Br 2 " " 62 " Br H OC.sub.2 H.sub.5 " " CH.sub.3 2 " greenish blue 63 CN H H H CH.sub.2 CH.sub.3 CH.sub.2 CH.sub.3CH.sub.3 2 COO violet 64 " H H H " " C.sub.2 H.sub.5 2 " " 65 " Br H H " " " 2 " blue 66 " Br H H " " CH.sub.3 2 " " 67 " Cl H H " " CH.sub.2 CH.sub.2 OCH.sub.3 2 " " 68 " Br H H " " " 2 " " 69 NO.sub.2 Br H OC.sub.2 H.sub.5 " " " 2 CO greenish blue 70 " " H " " " C.sub.2 H.sub.5 2 " " 71 " " H " " " CH(CH.sub.3).sub.2 2 " " 72 " " H " " " CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.3 2 " " 73 " " H " " " CH.sub.2 CH.sub.2 OC.sub.2 H.sub.5 2 " " 74 NO.sub.2 Cl H OC.sub.2 H.sub.5 CH.sub.2 CH.sub.2 OCOC.sub.2 H.sub.5 CH.sub.2 CH.sub.2 OCOC.sub.2 H.sub.5 CH.sub.3 3 CO reddish blue 75 " Br H " C.sub.2 H.sub.5 C.sub.2 H.sub.5 CH.sub.2 CH.sub.2 OCH(CH.sub.3).sub.2 2 " greenish blue 76 " Br H " " CH.sub.2 CH.sub.2 COOC.sub.2 H.sub.5 CH.sub.3 2 " blue 77 " " H " " CH.sub.2 CH.sub.2 COOCH.sub.2 CH.sub.2 CH.sub.2 CH.sub.3 " 2 " " 78 " Br H " CH.sub.2 CH.sub.2 COOC.sub.2 H.sub.5 CH.sub.2 CH.sub.2 OH CH.sub.2 CH.sub.2 CH.sub.3 2 " " 79 " " H " C H.sub.2 CH.sub.2 COOCH.sub.2 CH.sub.2 CH.sub.3 " " 2 " " 80 " Cl H " CH.sub.2 CH.sub.2 COOCH.sub.3 CH.sub.3 CH.sub.3 2 " blue 81 " Br H " CH.sub.2 CH.sub.2 CO.sub.2 C.sub.2 H.sub.5 C.sub.2 H.sub.5 " 2 SO.sub.2 " 82 " Br H " C.sub.2 H.sub.5 ##STR15## " 2 COO " 83 NO.sub.2 Cl H OC.sub.2 H.sub.5 CH.sub.2 CH.sub.2 OCHO CH.sub.2 CH.sub.2 OCHO CH.sub.3 2 CO reddish blue 84 " Cl H " CH.sub.2 CH.sub.2 OCOC.sub.2 H.sub.5 CH.sub.2 CH.sub.2 OCOC.sub.2 H.sub.5 " 2 " " 85 " Br H " CH.sub.2 CH.sub.2 OCOCH.sub.2 CH.sub.2 CH.sub.3 CH.sub.2 CH.sub.2 OCOCH.sub.2 CH.sub.2 CH.sub.3 " 2 " blue 86 " Br H " C.sub.2 H.sub.5 C.sub.2 H.sub.5 CH.sub.2 CH.sub.2 CN 2 " " 87 " Br H " " " CH.sub.2 CH.sub.2 Cl 2 " " 88 " Br H " " " CH.sub.2 CH.sub.2 Br 2 " " 89 " Br H " " " CH.sub.2 CH.sub.2 OCH.sub.3 2 COO greenish blue 90 " Br H " " " CH.sub.2 CH.sub.2 C.sub.2 H.sub.5 2 " " 91 " Br H " CH.sub.2 CH.sub.2 OCOCH.sub.3 CH.sub.2 CH.sub.2 OCOCH.sub.3 " 2 " reddish blue 92 " Br H " " " CH.sub.2 CH.sub.2 OCH.sub.3 2 " " 93 " Cl H " " " " 2 " " 94 " Br H " C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.5 2 " blue
APPLICATION EXAMPLE
A mixture of 7 parts of the dye produced as in the foregoing Example 2, 4 parts of sodium dinaphthylmethane disulphonate, 4 parts of sodium cetyl sulphate and 5 parts of anhydrous sodium sulphate is ground in a ball mill for 48 hours to give a fine powder. One part of the powder is dispersed in a little water and the dispersion run through a sieve into a bath of 4000 parts of water containing 2 parts of sodium lauryl sulphate.
100 Parts of a scoured polyester fabric are entered into this dyebath (goods to liquor ratio 1:40) at 40.degree.-50.degree., after which 20 parts of an emulsion of a chlorinated benzene in water are added. The bath is raised slowly to 100.degree. and the fabric dyed for 1-2 hours at 95.degree.-100.degree.. On removal it is rinsed, soaped, rinsed and dried. A level blue dyeing of good depth is obtained which is outstandingly fast to light, washing, water, sea water, perspiration, sublimation, gas fumes, thermofixation, pleating, cross dyeing and permanent press finishing.
Formulae of representative dyestuffs of the foregoing Examples are as follows: ##STR16##

Claims

1. A compound of the formula
wherein
R.sub.1 is nitro, cyano, phenylsulfonyl or tolylsulfonyl,
R.sub.2 is hydrogen, chloro or bromo,
R.sub.13 is hydrogen, formamido, acetamido, propionamido, chloropropionamido or bromopropionamido, with the proviso that at least one of R.sub.2 and R.sub.13 is hydrogen,
R.sub.14 is hydrogen, methoxy or ethoxy,
R.sub.25 is alkyl, cyanoalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.26 is alkyl, hydroxyalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.27 is alkoxyalkyl,
X is --CO--, --CO.sub.2 -- or --SO.sub.2 --, and
m is 2 or 3,
wherein each alkyl, hydroxyalkyl and alkyl and alkoxy radical of each cyanoalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl, alkoxycarbonylalkyl and alkoxyalkyl independently has 1 to 4 carbon atoms
2. A compound according to claim 1 having the formula ##STR17## wherein R.sub.2 is hydrogen, chloro or bromo,
R.sub.14 is hydrogen, methoxy or ethoxy,
R.sub.21 is cyano, phenylsulfonyl or tolylsulfonyl,
R.sub.25 is alkyl, cyanoalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.26 is alkyl, hydroxyalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.27 is alkoxyalkyl,
X is --CO--, --CO.sub.2 -- or --SO.sub.2 --, and
m is 2 or 3,
wherein each alkyl, hydroxyalkyl and alkyl and alkoxy radical of each cyanoalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl, alkoxycarbonylalkyl and alkoxyalkyl independently has 1 to 4 carbon atoms.
3. A compound according to claim 2 wherein R.sub.27 is .beta.-alkoxyethyl.
4. A compound according to claim 3 wherein
R.sub.14 is hydrogen,
R.sub.21 is cyano,
X is --CO--, and
m is 2.
5. A compound according to claim 1 having the formula ##STR18## wherein R.sub.2 is hydrogen, chloro or bromo,
R.sub.13 is hydrogen, formamido, acetamido, propionamido, chloropropionamido or bromopropionamido, with the proviso that at least one of R.sub.2 and R.sub.13 is hydrogen
R.sub.14 is hydrogen, methoxy or ethoxy,
R.sub.25 is alkyl, cyanoalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.26 is alkyl, hydroxyalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl,
R.sub.27 is alkoxyalkyl,
X is --CO--, --CO.sub.2 -- or --SO.sub.2 --, and
m is 2 or 3,
wherein each alkyl, hydroxyalkyl and alkyl and alkoxy radical of each cyanoalkyl, formyloxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl, alkoxycarbonylalkyl and alkoxyalkyl independently has 1 to 4 carbon atoms.
6. A compound according to claim 5 wherein R.sub.27 is .beta.-alkoxyethyl.
7. A compound according to claim 6 wherein
R.sub.13 is hydrogen,
R.sub.14 is ethoxy,
R.sub.25 is ethyl or .beta.-acetoxyethyl,
R.sub.26 is ethyl or .beta.-acetoxyethyl,
X is --CO-- or --CO.sub.2 --, and
m is 2,
8. The compound according to claim 7 having the formula ##STR19##
9. The compound according to claim 7 having the formula ##STR20##
10. The compound according to claim 7 having the formula ##STR21##
11. The compound according to claim 7 having the formula ##STR22##
12. The compound according to claim 7 having the formula ##STR23##
13. The compound according to claim 7 having the formula ##STR24##
14. The compound according to claim 3 having the formula ##STR25##
15. The compound according to claim 3 having the formula ##STR26##
16. The compound according to claim 3 having the formula ##STR27##
17. The compound according to claim 3 having the formula ##STR28##
18. The compound according to claim 3 having the formula ##STR29##
19. The compound according to claim 3 having the formula ##STR30##

Priority Claims (2)

Number	Date	Country	Kind
6808/70	May 1970	CH
19249/70	Dec 1970	CH

Parent Case Info

This application is a continuation of application Ser. No. 337,273, filed Mar. 1, 1973 and now abandoned, which, in turn, is a continuation-in-part of application Ser. No. 138,813, filed Apr. 29, 1971 and now abandoned.

US Referenced Citations (7)

Number	Name	Date
3268507	Kruckenberg	Aug 1966
3342804	Mueller	Sep 1962
3359256	Mueller et al.	Dec 1967
3398135	Mueller	Aug 1968
3398137	Mueller	Aug 1968
3428622	Altermatt et al.	Feb 1969
3652534	Wegmuller	Mar 1972

Foreign Referenced Citations (2)

Number	Date	Country
766,772	Jun 1971	BE
1,928,372	Feb 1970	DT

Continuations (1)

	Number	Date	Country
Parent	337273	Mar 1973

Continuation in Parts (1)

	Number	Date	Country
Parent	138813	Apr 1971

Phenylazophenyl dyes having an alkoxyacylamino group on the coupling component radical

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

US Classifications

Field of Search

US

International Classifications

Abstract