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Monoazo dyestuffs of the benzene-azo-pyrazolone series and metal complexes thereof

机译:苯-偶氮-吡唑啉酮系列的单偶氮染料及其金属配合物

摘要

Compounds of formula (enol form) FORM:0806709/IV (b)/1 wherein Y is an alkyl, aryl, CONH2, CONH (alkyl), CON(alkyl)2 or CO.O.alkyl group, Z is hydrogen or a substituent other than a sulphonic or carboxylic acid group, and R1 is a methylene or o-arylene radical may be prepared by converting heterocyclic ether sulphones containing amino groups (cf. Specification 753,261) via their diazo compounds into the corresponding hydrazines and condensing the latter with, for example, acetoacetic, benzoylacetic or oxalacetic acid esters to give the corresponding pyrazolones. They are used as coupling components in the manufacture of azo dyestuffs (see Group IV (c)). Specified compounds are of the above formula wherein Y=CH3, Z=H, Cl or CH3 and R1=CH2; Y=CONH2, CON(CH3)2, CO.O.C2H5 or C6H5, Z=H and R1=CH2; Y=CH3, Z=H and R1=4-chloro-1 : 2-phenylene. Specification 731,495 also is referred to.ALSO:The invention comprises monoazo dyestuffs of formula FORM:0806709/IV (c)/1 wherein R is a radical of the benzene series free from sulphonic acid and non-complex forming carboxylic acid groups, X is a group capable of forming a metal complex ortho to -N = N-, Y is alkyl, aryl, -CONH2, CONH(alkyl), CON (alkyl)2 or CO.O.alkyl, Z is hydrogen or a substituent other than a sulphonic or carboxylic acid group and R1 is methylene or an o-arylene radical; and the metal complexes thereof. The dyestuffs are prepared by coupling a diazotized aminobenzene, which is substituted as defined above with a pyrazolone of formula FORM:0806709/IV (c)/2 wherein Y, Z and R1 are as defined above. The preferred metal complexes are the chromium and cobalt complexes. They are prepared by treating the dyestuffs with chromium- or cobalt-yielding agents in known manner, preferably so as to yield 2 : 1 complexes. A mixture of two different dyestuffs of formula (I) or a dyestuff of formula (I) and another known metallizable monoazo dyestuff may also be metallized, possibly by formation of the 1 : 1 complex of one of the dyestuffs and reaction of this complex with the other dyestuff. Specified components in addition to those specified in examples are: diazo components: 2-aminophenol, 1-amino-2 - hydroxy - 4 - or 5 - chlorobenzene, 1 - amino-2 - hydroxy - 3 : 5 - dichloro - or dinitro - benzene, 1 - amino - 2 - hydroxy - 3 - nitro - or chloro - 5 - nitro - or chloro - benzene, 1-amino - 2 - hydroxy - 3 - methyl - 5 - nitrobenzene, 1 - amino - 2 - hydroxybenzene - 5 - sulphopiperidide or sulphomorpholide or sulphoanilide or sulphoethylamide, 1-amino-2-hydroxy-3-chlorobenze - 5 - sulphonamide and anthranilic acid - sulphonamides; coupling components: compounds of formula (II) wherein Y = CONH2 or CO.OC2H5, Z = H and R1 = CH2. The metal complexes may be used to colour resins, lacquers and plastic masses and to dye leather, wool and synthetic polyamides and polyurethanes. They dye wool in red or yellow shades. In examples: (1) the diazo compound from 1 - amino - 2 - hydroxy - or methoxy - 5-sulphonamide, 1 - amino - 2 - hydroxy - 4 - or 5 - nitrobenzene, 1 - amino - 2 - hydroxy - 5-methyl - 3 - nitrobenzene, 1 - amino - 2 - hydroxybenzene - 5 - ethyl - or n - propyl - sulphone, 3 - amino - 4 - hydroxy - diphenylsulphone - (1 : 11), 1 - amino - 2 - hydroxybenzene-5 - sulpho - methylamide or dimethylamide, 1-amino - 2 - hydroxybenzene - 5 - sulpho - methyl-b - hydroxyethylamide, 1 - amino - 2 - hydroxybenzene - 4 - sulphonamide or sulphomethylamide, 1 - amino - 2 - hydroxy - 5 - chlorobenzene - 3 - sulphonamide, anthranilic acid or 4-amino - 5 - hydroxybenzoxathiol - S - dioxide is coupled with the compound of formula (II) wherein Y = CH3, Z = H and R1 = CH2, the chromium and cobalt complexes of the dyestuffs being prepared; (2) the diazo compound from 1 - amino - 2 - hydroxy - or methoxybenzene - 5 - sulphonamide is coupled with a compound of formula (II) wherein Y = CH3, Z = Cl or CH3 and R1 = CH2 or Y = phenyl, Z = H and R1 = CH2 or Y = CON(CH3)2, Z = H and R1 = CH2 or Y = CH3, Z = H and R1 = 4-chloro-1 : 2-phenylene and the cobalt and chromium complexes of the dyestuffs are prepared; (3) the chromium complex of a mixture of dyestuffs, i.e. 1-amino-2-hydroxybenzene-5-sulphonamide -- compound of formula (II) wherein Y = CH3, Z = Cl and R1 = CH2 and 1 - amino - 2 - hydroxy - 5 - nitrobenzene -- compound of formula (II) wherein Y = CH3, Z = H and R1 = CH2 is prepared; (4) the cobalt complex of a mixture of dyestuffs as in (3), except that the diazo compound of the second dyestuff is 1-amino-2-hydroxybenzene-5-sulphodimethylamide, is prepared; (5) the chromium and cobalt complexes of a mixture of dyestuffs, i.e. 1 - amino - 2 - hydroxybenzene-5 - ethylsulphone -- compound of formula (II) wherein Y = CH3, Z = H and R1 = CH2 and 1 - amino - 2 - hydroxy - 5 - nitrobenzene -- 2 - hydroxy - 8 - methylsulphonylamino-naphthalene are prepared. Specifications 681,653, [731,495, 753,261] [both in Group IV (b)], 758,016 and 766,554 are referred to.
机译:式(烯醇形式)的化合物,其中Y为烷基,芳基,CONH2,CONH(烷基),CON(烷基)2或CO.O.烷基,Z为氢R 1为亚甲基或邻亚芳基,可以通过将含氨基的杂环醚砜(参见规格753,261)通过其重氮化合物转化为相应的肼并将其缩合而制得R1为亚甲基或邻亚芳基。后者与例如乙酰乙酸酯,苯甲酰乙酸酯或草酰乙酸酯一起得到相应的吡唑啉酮。它们在偶氮染料的生产中用作偶联组分(请参阅第IV(c)组)。特定的化合物具有上式,其中Y = CH 3,Z = H,Cl或CH 3且R 1 = CH 2。 Y = CONH 2,CON(CH 3)2,CO 2 O 5或C 6 H 5,Z = H且R 1 = CH 2; Y = CH 3,Z = H且R 1 = 4-氯-1:2-亚苯基。还参考说明书731,495。ALSO:本发明包括式的单偶氮染料,其中R是不含磺酸和非络合物形成羧酸基团的苯系列基团, X是能够形成与-N = N-相邻的金属络合物的基团,Y是烷基,芳基,-CONH 2,CONH(烷基),CON(烷基)2或CO.O.烷基,Z是氢或取代基除磺酸基或羧酸基以外,R 1为亚甲基或邻亚芳基。及其金属配合物。通过将重氮化的氨基苯如上定义被式的吡唑啉酮偶联来制备染料,其中Y,Z和R 1如上定义。优选的金属配合物是铬和钴配合物。它们通过以已知方式用铬或钴生成剂处理染料来制备,优选以产生2∶1的配合物的方式进行。两种不同的式(I)的染料或式(I)的染料与另一种已知的可金属化的单偶氮染料的混合物也可以被金属化,可能是通过形成一种染料的1:1络合物并使该络合物与其他染料。除实例中指定的组分外,指定的组分还有:重氮组分:2-氨基苯酚,1-氨基-2-羟基-4-或5-氯苯,1-氨基-2-羟基-3:5-二氯或二硝基-苯,1-氨基-2-羟基-3-硝基或氯-5-硝基或氯-苯,1-氨基-2-羟基-3-甲基-5-硝基苯,1-氨基-2-羟基苯- 5-磺基哌啶或磺基吗啉化物或磺酰苯胺或磺基乙酰胺,1-氨基-2-羟基-3-氯苯甲酸-5-磺酰胺和邻氨基苯甲酸-磺酰胺;偶合组分:式(II)的化合物,其中Y = CONH 2或CO.OC 2 H 5,Z = H且R 1 = CH 2。该金属络合物可用于为树脂,清漆和塑料块着色,以及为皮革,羊毛和合成聚酰胺和聚氨酯染色。他们将羊毛染成红色或黄色。在实例中:(1)重氮化合物,其选自1-氨基-2-羟基或甲氧基5-磺酰胺,1-氨基-2-羟基-4-或5-硝基苯,1-氨基-2-羟基-5甲基-3-硝基苯,1-氨基-2-羟基苯-5-乙基或正丙基-砜,3-氨基-4-羟基-二苯砜-(1:11),1-氨基-2-羟基苯-5 -磺基-甲基酰胺或二甲基酰胺,1-氨基-2-羟基苯-5-磺基-甲基-b-羟乙基酰胺,1-氨基-2-羟基苯-4-磺酰胺或磺基甲基酰胺,1-氨基-2-羟基-5-氯苯-3-磺酰胺,邻氨基苯甲酸或4-氨基-5-羟基苯并恶硫醇-S-二氧化物与式(II)化合物(其中Y = CH 3,Z = H且R 1 = CH 2),染料的铬和钴配合物偶联正在准备; (2)将1-氨基-2-羟基或甲氧基苯-5-磺酰胺中的重氮化合物与式(II)化合物偶合,其中Y = CH3,Z = Cl或CH3,R1 = CH2或Y =苯基, Z = H且R1 = CH2或Y = CON(CH3)2,Z = H且R1 = CH2或Y = CH3,Z = H且R1 t = 4-氯-1:2-亚苯基以及钴和铬制备染料的配合物; (3)染料混合物的铬配合物,即1-氨基-2-羟基苯-5-磺酰胺->式(II)的化合物,其中Y = CH3,Z = Cl且R1 = CH2,并且1-氨基-制备式(Ⅱ)的2-羟基-5-硝基苯化合物,其中Y = CH 3,Z = H,R 1 = CH 2。 (4)除第二染料的重氮化合物为1-氨基-2-羟基苯-5-磺基二甲酰胺外,制备(3)的染料混合物的钴配合物。 (5)染料混合物的铬和钴配合物,即1-氨基-2-羟基苯5-乙基砜->式(II)的化合物,其中Y = CH3,Z = H和R1 = CH2和1-制备了氨基-2-羟基-5-硝基苯-> 2-羟基-8-甲基磺酰基氨基-萘。规格681,653,[731,495、753,261] [都属于第IV(b)组],758,016和766,554。

著录项

  • 公开/公告号GB806709A

    专利类型

  • 公开/公告日1958-12-31

    原文格式PDF

  • 申请/专利权人 FARBENFABRIKEN BAYER AKTIENGESELLSCHAFT;

    申请/专利号GB19560012217

  • 发明设计人

    申请日1956-04-20

  • 分类号C09B45/14;

  • 国家 GB

  • 入库时间 2022-08-23 19:49:10

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