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Manufacture of new amine derivatives and application thereof in industrial processes, in particular as optical bleaching agents

机译:新胺衍生物的制造及其在工业过程中的应用,特别是作为光学漂白剂的应用

摘要

Water-solubilizing groups are introduced into the amino group of a blue-fluorescent compound (other than an amino-coumarin or an amino-naphthalene sulphonic acid) by treating it with (a) an aldehyde bisulphite or with an aldehyde and sulphur dioxide, or (b) an alkyl or aralkyl halide containing at least one sulphonic or carboxylic acid group preferably in the presence of an p acid-binding agent, or (c) the addition product of pyridine and sulphur dioxide, or (d) an N-methylolamide of a carboxylic acid with at least one water-solubilizing group in the acyl radical or a mixture of formaldehyde and an amide of such a carboxylic acid, or (e) a mercapto compound which contains a water-solubilizing group in the presence of an aldehyde or acetal. Suitable blue-fluorescent starting materials are 1,5-naphthylene - diamine, 4 - amino - acenaphthene, 3 - amino - pyrene, 2 - amino - crysene, 4,41-diaminostilbene - 2,21 - disulphonic acid and its 4 - aminobenzoyl and 4 - (41 - aminobenzoylamino) - benzoyl derivatives, 2 - (41 - aminophenyl) - 6 - methyl benzothiazole and 2-(41 - aminophenyl) - benzimidazole. The products may be used for whitening undyed material or for brightening dyed material, and may be applied together with soaps or other washing agents such as salts of sulphonated fatty compounds. In examples: (1) 2-(41-aminophenyl) - 6 - methylbenzothiazole (compound I) is reacted with formaldehyde disulphite solution; (2) 4,41-bis-(411-aminobenzoylamino) - stilbene - 2,21 - disulphonic acid (compound II) is reacted with formaldehyde bisulphite; (3) compound II is reacted with chlorsulphonic acid in the presence of pyridine; (4) compound II is reacted with mono-chloracetic acid; (5) 3-aminopyrene or 3-aminochrysene is reacted with formaldehyde bisulphite; (6) 4-amino-41-(aminobenzoylamino)-2,21-disulphonic acid is reacted with formaldehyde bisulphite; (7) compound II is reacted with formaldehyde and thioglycollic acid; (8) the compound obtained by reducing the reaction product of benzidine-3,31-disulphonic acid and p-nitro-benzoyl chloride is reacted with formaldehyde bisulphite; (9) compound II is reacted with benzaldehyde bisulphite; (10) compound II is reacted with furfurol bisulphite; (11) compound I is reacted with chlorosulphonic acid in the presence of pyridine; (12) 2-(41-aminophenyl)-6-methylbenzothiazole monosulphonic acid (obtained by sulphonation of compound I with fuming sulphuric containing 10 per cent of sulphur trioxide at 20-25 DEG C.) is reacted with benzaldehyde bisulphite; (13) compound I is reacted with furfurol bisulphite; (14) 2-(41-aminophenyl)-benzimidazole is reacted with formaldehyde bisulphite; (15) compound I is reacted with the quarternary addition product of trimethylamine and N-methylol-chloracetamide; and (16) the condensation product obtained from 4,41-diaminostilbene-2,21-disulphonic acid, cyanuric chloride, aniline and ammonia is reacted with formaldehyde bisulphite.ALSO:Water-solubilizing groups are introduced into the amino group of a blue-fluorescent compound (other than an amino-coumarin or an amino-naphthalene sulphonic acid) by treating it with (a) an aldehyde bisulphite or with an aldehyde and sulphur dioxide; or (b) an alkyl or aralkyl halide containing at least one sulphonic or carboxylic acid group, preferably in the presence of an acid-binding agent; or (c) the addition product of pyridine and sulphur dioxide; or (d) an N-methylolamide of a carboxylic acid with at least one water-solubilizing group in the acyl radical or a mixture of formaldehyde and an amide of such a carboxylic acid; or (e) a mercapto compound which contains a water-solubilizing group in the presence of an aldehyde or acetal. Suitable blue-fluorescent starting materials are 1,5 - naphthylene - diamine, 4 - amino - acenaphthene, 3 - amino - pyrene, 2 - amino - crysene, 4,41 - diaminostilbene - 2,21 - disulphonic acid and its 4-aminobenzoyl and 4 - (41 - aminobenzoyl - amino) - benzoyl derivatives, 2 - (41 - aminophenyl) - 6 - methyl benzothiazole and 2-(41-aminophenyl)-benzimidazole. The products may be used for whitening undyed material or for brightening dyed material, and may be applied together with soaps or other washing agents such as salts of sulphonated fatty compounds. In examples: (1) 2-(41-aminophenyl) - 6 - methyl - benzothiazole (compound I) is reacted with formaldehyde disulphite solution; (2) 4,41 - bis - (411 - aminobenzoylamino) - stilbene - 2,21 - disulphonic acid (compound II) is reacted with formaldehyde bisulphite; (3) compound II is reacted with chlorosulphonic acid in the presence of pyridine; (4) compound II is reacted with monochloracetic acid; (5) 3-aminopyrene or 3-aminochrysene is reacted with formaldehyde bisulphite; (6) 4 - amino - 41 - (aminobenzoylamino) - 2,21 - disulphonic acid is reacted with formaldehyde bisulphite; (7) compound II is reacted with formaldehyde and thioglycollic acid; (8) the compound obtained by reducing the reaction product of benzidine-3,31-disulphonic acid and p-nitro-benzoyl chloride is reacted with formaldehyde bisulphite; (9) compound II is reacted with benzaldehyde bisulphite; (10) compound II is reacted with furfurol bisulphite; (11) compound I is reacted with chlorosulphonic acid in the presence of pyridine; (12) 2-(41-aminophenyl)-6-methylbenzothiazole monosulphonic acid (obtained by sulphonation of compound I with fuming sulphuric containing 10 per cent of sulphur trioxide at 20-25 DEG C.) is reacted with benzaldehyde bisulphite; (13) compound I is reacted with furfurol bisulphite; (14) 2-(41-aminophenyl)-benzimidazole is reacted with formaldehyde bisulphite; (15) compound I is reacted with the quarternary addition product of trimethylamine and N-methylol-chloracetamide; (16) the condensation product obtained from 4,41 - diaminostilbene - 2,21 - disulphonic acid, cyanuric chloride, aniline and ammonia is reacted with formaldehyde bisulphite; (17) the product of (2) is mixed with soap and used for washing textiles; (18) silk is whitened by treatment with the product of (1) in presence of acetic acid; (19) cotton is whitened by treatment with the product of (7); (20) acetate artificial silk is whitened by treatment with the product of (1); (21) a paper of high degree of whiteness is obtained by adding the product of (2) to the pulp in a hollander together with resin size and aluminium sulphate; (22) cellulose fabric dyed with a triazo dye is printed with a discharge containing sodium formaldehyde sulphoxylate and the product of (2); and (23) staple fibres of regenerated cellulose are treated with a bath usual for crease-proofing to which is added the product of (2).ALSO:Water-solubilizing groups are introduced into the amino group of a blue-fluorescent compound (other than an amino-coumarin or an aminonaphthalene sulphonic acid) by treating it with (a) an aldehyde bisulphite or with an aldehyde and sulphur dioxide; or (b) an alkyl or aralkyl halide containing at least one sulphonic or carboxylic acid group preferably in the presence of an acid-binding agent; or (c) the addition product of pyridine and sulphur dioxide; or (d) an N-methylolamide of a carboxylic acid with at least one water-solubilizing group in the acyl radical or a mixture of formaldehyde and an amide of such a carboxylic acid; or (e) a mercapto compound which contains a water-solubilizing group in the presence of an aldehyde or acetal. Suitable blue-fluorescent starting materials are 1,5 - naphthylene - diamine, 4 - amino-acenaphthene, 3-amino-pyrene, 2-amino-crysene, 4,41-diaminostilbene-2,21-disulphonic acid and its 4-aminobenzoyl and 4-(41-aminobenzoyl - amino) - benzoyl derivatives, 2 - (41 - aminophenyl) - 6 - methyl benzothiazole and 2 - (41 - aminophenyl) - benzimidazole. The products may be used for whitening undyed material or for brightening dyed material, may be applied together with soaps or other washing agents such as salts of sulphonated fatty compounds. In example (17) the condensation product of 4,41-bis-(411-aminobenzoyl-amino)-stilbene-2, 21-disulphonic acid and formaldehyde bisulphite is mixed with soap and used for washing textiles.
机译:通过用(a)醛亚硫酸氢盐或醛和二氧化硫处理,将水溶性基团引入蓝色荧光化合物的氨基(氨基香豆素或氨基萘磺酸除外)中。 (b)含有至少一个磺酸或羧酸基团的烷基或芳烷基卤化物,优选在对酸结合剂的存在下,或(c)吡啶和二氧化硫的加成产物,或(d)N-羟甲基酰胺在酰基或甲醛与这种羧酸的酰胺的混合物中具有至少一个水溶性基团的羧酸,或(e)在醛存在下含有水溶性基团的巯基化合物或缩醛。合适的蓝色荧光起始材料是1,5-亚萘基-二胺,4-氨基-,3-氨基-,、 2-氨基-s烯,4,41-二氨基sti-2,21-二磺酸及其4-氨基苯甲酰基。和4-(41-氨基苯甲酰基氨基)-苯甲酰基衍生物,2-(41-氨基苯基)-6-甲基苯并噻唑和2-(41-氨基苯基)-苯并咪唑。该产品可用于增白未染色的材料或增白染色的材料,并可与肥皂或其他洗涤剂(如磺化脂肪化合物的盐)一起使用。在实施例中:(1)使2-(41-氨基苯基)-6-甲基苯并噻唑(化合物I)与亚硫酸氢甲醛溶液反应; (2)使4,41-双-(411-氨基苯甲酰氨基)--2,21-二磺酸(化合物II)与甲醛合亚硫酸氢盐反应; (3)使化合物Ⅱ在吡啶存在下与氯磺酸反应。 (4)使化合物Ⅱ与一氯乙酸反应; (5)使3-氨基py或3-氨基ch与甲醛合亚硫酸氢盐反应; (6)使4-氨基-41-(氨基苯甲酰基氨基)-2,21-二磺酸与甲醛合亚硫酸氢盐反应; (7)使化合物Ⅱ与甲醛和巯基乙酸反应。 (8)使通过还原3,31-联苯甲酸和对硝基-苯甲酰氯的反应产物得到的化合物与甲醛亚硫酸氢盐反应; (9)使化合物Ⅱ与苯甲醛亚硫酸氢盐反应; (10)使化合物Ⅱ与糠醇亚硫酸氢盐反应; (11)化合物I在吡啶的存在下与氯磺酸反应; (12)使2-(41-氨基苯基)-6-甲基苯并噻唑单磺酸(通过在20-25℃下用含10%三氧化硫的发烟硫酸磺化化合物I而得到)与苯甲醛亚硫酸氢盐反应; (13)使化合物I与糠醇亚硫酸氢盐反应; (14)使2-(41-氨基苯基)-苯并咪唑与甲醛合亚硫酸氢盐反应; (15)使化合物I与三甲胺和N-羟甲基-氯乙酰胺的季铵加成产物反应; (16)将4,41-二氨基二苯乙烯-2,21-二磺酸,氰尿酰氯,苯胺和氨水制得的缩合产物与甲醛合亚硫酸氢盐反应。ALSO:水溶性基团被引入到荧光化合物(氨基香豆素或氨基萘磺酸除外)通过以下方式处理:(a)醛亚硫酸氢盐或醛和二氧化硫; (b)含有至少一个磺酸或羧酸基团的烷基或芳烷基卤化物,优选在酸结合剂的存在下;或(c)吡啶与二氧化硫的加成产物;或(d)在酰基中具有至少一个水溶性基团的羧酸的N-羟甲基酰胺,或甲醛与这种羧酸的酰胺的混合物;或(e)在醛或乙缩醛的存在下含有水溶性基团的巯基化合物。合适的蓝色荧光起始材料是1,5-亚萘基-二胺,4-氨基-,3-氨基-pyr,2-氨基-s烯,4,41-二氨基sti-2,21-二磺酸及其4-氨基苯甲酰基。和4-(41-氨基苯甲酰基-氨基)-苯甲酰基衍生物,2-(41-氨基苯基)-6-甲基苯并噻唑和2-(41-氨基苯基)-苯并咪唑。该产品可用于增白未染色的材料或增亮染色的材料,并可与肥皂或其他洗涤剂(如磺化脂肪化合物的盐)一起使用。在实施例中:(1)使2-(41-氨基苯基)-6-甲基-苯并噻唑(化合物I)与亚硫酸氢甲醛溶液反应; (2)使4,41-双-(411-氨基苯甲酰氨基)-苯乙烯-2,21-二磺酸(化合物II)与甲醛合亚硫酸氢盐反应; (3)使化合物II在吡啶存在下与氯磺酸反应; (4)使化合物Ⅱ与一氯乙酸反应; (5)使3-氨基py或3-氨基ch与甲醛合亚硫酸氢盐反应; (6)使4-氨基-41-(氨基苯甲酰氨基)-2,21-二磺酸与甲醛合亚硫酸氢盐反应; (7)使化合物Ⅱ与甲醛和巯基乙酸反应。 (8)通过还原联苯胺-3的反应产物获得的化合物,31-二磺酸与对硝基苯甲酰氯与甲醛合亚硫酸氢盐反应; (9)使化合物Ⅱ与苯甲醛亚硫酸氢盐反应; (10)使化合物Ⅱ与糠醇亚硫酸氢盐反应; (11)化合物I在吡啶的存在下与氯磺酸反应; (12)使2-(41-氨基苯基)-6-甲基苯并噻唑单磺酸(通过在20-25℃下用含10%三氧化硫的发烟硫酸磺化化合物I而得到)与苯甲醛亚硫酸氢盐反应; (13)使化合物I与糠醇亚硫酸氢盐反应; (14)使2-(41-氨基苯基)-苯并咪唑与甲醛合亚硫酸氢盐反应; (15)使化合物I与三甲胺和N-羟甲基-氯乙酰胺的季铵加成产物反应; (16)使由4,41-二氨基二苯乙烯-2,21-二磺酸,氰尿酰氯,苯胺和氨获得的缩合产物与甲醛合亚硫酸氢盐反应; (17)将(2)的产物与肥皂混合并用于洗涤纺织品; (18)通过在乙酸存在下用(1)的产物处理来使丝绸变白; (19)用(7)的产品处理使棉花变白; (20)用(1)的产物处理使乙酸人造丝变白。 (21)通过将(2)的产物与树脂胶料和硫酸铝一起加入到荷兰兰德的纸浆中获得高白度的纸; (22)将用三偶氮染料染色的纤维素织物印刷上含有甲醛次硫酸氢钠和(2)产物的排料。 (23)将再生纤维素的短纤维用通常用于防皱的浴处理,并加入(2)的产物。将ALSO:水溶性基团引入蓝色荧光化合物的氨基中(其他比氨基香豆素或氨基萘磺酸),可通过以下方法处理:(a)醛亚硫酸氢盐或醛和二氧化硫; (b)含有至少一个磺酸或羧酸基的烷基或芳烷基卤化物,优选在酸结合剂存在下;或(c)吡啶与二氧化硫的加成产物;或(d)在酰基中具有至少一个水溶性基团的羧酸的N-羟甲基酰胺,或甲醛与这种羧酸的酰胺的混合物;或(e)在醛或乙缩醛的存在下含有水溶性基团的巯基化合物。合适的蓝色荧光原料是1,5-萘-二胺,4-氨基-,3-氨基amino,2-氨基-,烯,4,41-二氨基amino-2,21-二磺酸及其4-氨基苯甲酰基。和4-(41-氨基苯甲酰基-氨基)-苯甲酰基衍生物,2-(41-氨基苯基)-6-甲基苯并噻唑和2-(41-氨基苯基)-苯并咪唑。该产品可用于增白未染色的材料或用于增亮染色的材料,可与肥皂或其他洗涤剂(如磺化脂肪化合物的盐)一起使用。在实施例(17)中,将4,41-双-(411-氨基苯甲酰基-氨基)-二苯乙烯-2、21-二磺酸和甲醛合亚硫酸氢盐的缩合产物与肥皂混合并用于洗涤织物。

著录项

  • 公开/公告号GB656590A

    专利类型

  • 公开/公告日1951-08-29

    原文格式PDF

  • 申请/专利权人 CIBA LIMITED;

    申请/专利号GB19480029813

  • 发明设计人

    申请日1948-11-16

  • 分类号

  • 国家 GB

  • 入库时间 2022-08-24 01:35:58

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