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process for faerben of regenerated cellulose in gleichmaessigen toenen

机译:格里希迈西希·蒂嫩的再生纤维素法尔本的制备方法

摘要

294,922. British Dyestuffs Corporation, Ltd., Baddiley, J., Chorley, P., and Brightman, R. April 28, 1927. Disazo dyes are obtained by coupling tetrazotized 2-nitro- or 2 : 21-dinitrobenzidine with two molecular proportions of a 2 : 8-aminonaphthol sulphonic acid or an N-derivative thereof or with one molecular proportion of such acid or derivative and one molecular proportion of any coupling component. The products in some cases yield even dyeings on regenerated cellulose silk, and in some cases yield dyeings fast to milling on wool. The following examples are specified :- (1) a dyestuff yielding red shades on viscose silk and wool is obtained by coupling 1 mol. of tetrazotized 2-nitrobenzidine with 1 mol. of salicylic acid (alkaline coupling) and 1 mol. of 2 : 8 . 6-acid (acid coupling); (2) a dyestuff yielding yellow-brown shades on viscose silk and wool is obtained by coupling 1 mol. of tetrazotized 2- nitrobenzidine with 1 mol. of 1-(21 : 51-dichloro- 4-sulpho) phenyl-3-methyl-5-pyrazolone (neutral coupling), and 1 mol. of 2: 8: 6-acid (alkaline coupling), and a dyestuff yielding redder shades is obtained from the same tetrazo compound with 2: 8: 6-acid and 1-(41-sulpho) phenyl-3-methyl-5- pyrazolone ; (3) a dyestuff yielding maroon shades on viscose silk and copper-brown shades on wool is obtained by coupling 1 mol. of tetrazotized 2- nitrobenzidine with 1 mol. of naphthionic acid (faintly acid coupling) and 1 mol. of phenyl- 2 : 8 : 6-acid (alkaline coupling) ; (4) a dyestuff yielding violet-brown shades on viscose silk and wool is obtained by coupling 1 mol. of tetrazotized 2-nitrobenzidine with 1 mol. of 2:8:6- acid (alkaline coupling) and 1 mol. of resorcinol or m-phenylenediamine, a dyestuff yielding violet shades on viscose silk and wool by replacing the second coupling component by 1 : 4-naphtholsulphonic acid, and a dyestuff yielding claret shades on viscose silk and reddish-brown shades on wool by coupling the tetrazo compound with 2 mols. of 2 : 8 : 6-acid; (5) a dyestuff vielding yellow-brown shades on viscose silk is obtained by coupling 1 mol. of tetrazotized 2 : 21-dinitrobenzidine with 1 mol. of salicyclic acid (alkaline coupling) and 1 mol. of 2 : 8 : 6-acid (alkaline coupling). A table is also given showing the shades on viscose silk with dyestuffs from tetrazotized 2-nitrobenzidine and various pairs of coupling components, other specified components being o- and p-cresotinic acids. 2 : 3-oxynaphthoic acid, benzoyl-2 : 8 : 6-acid, the glycine of 2 : 8 : 6- acid, ethyl-2: 8 : 6-acid. 21 : 4'-dinitrophenyl- 2 : 8 : 6-acid, 41-chlorophenyl-2 : 8 : 6-acid, and m-xylyl-2 : 8 : 6-acid. 2-(41-chlorophenyl)amino-8-naphthol-6-sulphonic acid is obtained by condensing p-chloraniline with 2 : 8 : 6-acid in presence of bisulphite.
机译:294,922。 British Dyestuffs Corporation,Ltd.,Baddiley,J.,Chorley,P.和Brightman,R. 1927年4月28日。双偶氮染料是通过将四唑基化的2-硝基-或2:2 1-二硝基联苯胺与两个分子偶联而获得的比例的2:8-氨基萘磺酸或其N-衍生物,或具有一分子比例的这种酸或衍生物和一分子比例的任何偶联组分。在某些情况下,产品在再生的纤维素丝上产生均匀的染色,在某些情况下,产生的速度快于在羊毛上进行研磨。规定了以下实施例:(1)通过偶联1mol获得在粘胶丝和羊毛上产生红色阴影的染料。 1mol。的四唑化2-硝基联苯胺水杨酸(碱性偶合剂)和1 mol。之2:8。 6-酸(酸耦合); (2)通过偶联1mol获得在粘胶丝和羊毛上产生黄棕色阴影的染料。 1mol的四唑基化2-硝基联苯胺。 1-(2 1:5 1-二氯-4-磺基)苯基-3-甲基-5-吡唑啉酮(中性偶合),和1摩尔。由相同的具有2:8:6-酸和1-(4 1 -sulpho)苯基-3-甲基的四唑化合物获得染料:产生2:8:6-酸(碱性偶合),并且染料产生红色阴影。 -5-吡唑酮; (3)通过偶联1mol获得在粘胶丝上产生栗色色调和在羊毛上产生铜棕色色调的染料。 1mol的四唑基化2-硝基联苯胺。萘甲酸(微弱的酸偶联)和1摩尔。苯基-2:8:6-酸(碱性偶合); (4)通过偶联1mol获得在粘胶丝和羊毛上产生紫褐色色调的染料。 1mol。的四唑化2-硝基联苯胺2:8:6-酸(碱性偶合)和1 mol。间苯二酚或间苯二胺的染料,通过将第二偶合组分替换为1:4-萘磺酸,在粘胶丝和羊毛上产生紫色调的染料,在粘胶丝上产生紫红色调的染料,在羊毛上产生红褐色调的染料2 mol四唑化合物。 2:8:6-酸; (5)通过偶联1mol获得在粘胶丝上呈现黄褐色阴影的染料。 1mol的四唑化的2:2 1-二硝基联苯胺。水杨酸(碱性偶联)和1mol。 2:8:6-酸(碱性偶合)还给出了一张表格,显示了粘胶丝上的色调,其带有来自四唑基化的2-硝基联苯胺的染料以及各种成对的偶合组分,其他指定的组分是邻-和对-甲苯磺酸。 2:3-氧萘甲酸,苯甲酰基-2:8:6-酸,甘氨酸2:8:6-酸,乙基-2:8:6-酸。 2 1:4'-二硝基苯基-2:8:6-酸,4 1-氯苯基-2:8:6-酸和间二甲苯基-2:8:6-酸。通过在亚硫酸氢盐的存在下将对氯苯胺与2:8:6-酸缩合,获得2-(4--氯苯基)氨基-8-萘酚-6-磺酸。

著录项

  • 公开/公告号DE000000539399A

    专利类型

  • 公开/公告日1931-11-25

    原文格式PDF

  • 申请/专利权人 ICI LTD;

    申请/专利号DEB0136960D

  • 发明设计人

    申请日1928-04-15

  • 分类号

  • 国家 DE

  • 入库时间 2022-08-24 08:04:55

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