DEC0010585MA - - Google Patents

Description

FEDERAL REPUBLIC OF GERMANY

Registration date: January 15, 1955 Announced on July 12, 1956

GERMAN PATENT OFFICE

PATENT APPLICATION

CLASS 12p GROUP 9 C 10585 IVb / 12p

Dr. Franz Ackermann, Binningen, and Dr. Adolf Emil Siegrist, Basel (Switzerland)

have been named as inventors

CIBA Aktiengesellschaft, Basel (Switzerland)

Representative: Dipl.-Ing. E. Splanemann, patent attorney, Hamburg 36

Process for the preparation of new imidazolium compounds

The priority of registrations in Switzerland from January 22nd and July 20th, 1954 ' is used

It has been found that new, valuable imidazolium compounds are obtained by using arylimidazoles the composition

A \ ■ / C ^^ R ₃ - C,

R ₁

.which both. A radicals are optionally substituted identical or different aromatic nuclei in which 2 vicinal carbon atoms are linked to the two imidazole _{nitrogen atoms, where R 1 is} hydrogen or an optionally substituted alkyl, aryl or aralkyl radical, R _{3 is} a divalent link with one or more conjugated double bonds, which form an uninterrupted series of conjugated double bonds with the yC == N double bonds of the imidazole rings, such as an ethylene radical or phenylene radical, or the salts of these imidazoles with

, 609 549/477

C 10585 IVb / 12 p

bonds that quaternize the ι imidazole nitrogen atom ability, in particular alkyl sulfates or aryl sulfonic acid alkyl esters, and optionally in a known manner one of 2 quaternary imidazole nitrogen atoms is dequaternized again and / or the anion of the imidazolium compound is exchanged for another anion.

As starting materials come in the present process, for. B. those connections into consideration,

ίο whose radicals A are naphthalene or, preferably, benzene nuclei. R ₁ can be an optionally further substituted phenyl radical, an aralkyl radical, such as, for. B. a benzyl radical or menaphthyl radical, but preferably a low molecular weight alkyl radical (e.g. a

Methyl, ethyl, propyl or butyl group, also an oxyalkyl group, such as oxyethyl) or ι be hydrogen atom.

The divalent link R ₃ can be of an aliphatic, aromatic, heterocyclic or araliphatic nature. For example, the following atom groupings are given for the link R ₃ .

-CH = CH-, -CH = CH-CH = CH-,
■ HC CH

-CH = CH

The imidazoles of the formula (1), the link of which R _{3 is} a simple ethylene bridge (- CH = CH -), generally lead to particularly valuable products. '

Compounds for quaternizing the imidazoles of the formula (1) are primarily the customary ones Alkylating and aralkylating agents into consideration. Examples include: methyl] odide, ethyl bromide, Isopropyl chloride, secondary butyl bromide, dodecyl bromide, epichlorohydrin, dimethyl sulfate, Benzyl halides and in the core z. B. benzyl halides substituted by halogen, alkyl or alkoxy groups, such as benzyl chloride, p-chlorobenzyl chloride, also menaphthyl chloride, toluenesulfonic acid esters, arylsulfonic acid alkyl esters, in particular those of Benzene series with low molecular weight alkyl groups, such as ethyl or methyl toluenesulfonate, continues Compounds that contain a water-solubilizing group, such as haloalkyl or aralkyl sulfonic acids, z. B. bromoethanesulfonic acid, benzyl chloride disulfonic acid. Unless of salts of imidazoles is assumed, alkylene oxides, such as ethylene oxide, propylene oxide or glycide, can also be used Quaternization can be used or, finally, low molecular weight aliphatic alcohols such as methanol or ethanol. The quaternization takes place under the usual conditions for such a reaction, expediently by heating the components to a higher temperature, e.g. B. 50 to 200 °, optionally vacuum. The use of inert solvents such as alcohols, e.g. B. methanol, ethyl alcohol, Dioxane, monomethylglycol, benzene, toluene, nitrobenzene or mixtures of such solvents, can be beneficial. It can optionally be advantageous to use an excess of quaternizing agents apply.

The imidazolium compounds obtainable by quaternizing the imidazoles of the formula (1) correspond to the formula

a:

, N.

(X ⁰ U (2)

in which both radicals A are identical or different, optionally substituted aromatic nuclei in which 2 vicinal carbon atoms are linked to the two imidazole nitrogen atoms, in which R is an optionally substituted alkyl or aralkyl radical, R _{1 is} hydrogen or an optionally substituted alkyl -, aryl or aralkyl radical, R ₃ for a divalent link which has at least one double bond which forms an uninterrupted series of conjugated double bonds with the ^> C = N double bonds of the imidazole rings, m for an integer with a value of at most two and X stands for an anion.

These new compounds show, in solution or applied to a substrate, in ultraviolet light green-blue to violet fluorescence and are therefore suitable as optical brighteners for materials such as Textiles and paper. For this purpose, the new compounds can already be added to a spinning mass or they can also be used as a lightening agent mixed with dyes, chemical bleaches, Use finishing agents or detergents.

In contrast to the salts formed with strong acids in the German patent 841 915 described N-monosubstituted diimidazoles, which are based on polyethylene terephthalate fibers ("Terylenes") the new quaternary imidazolium compounds do not produce a noticeable lightening effect a good lightening effect on terylene fabric.

In the following examples, unless otherwise noted, parts mean parts by weight; The relationship between parts by weight and parts by volume is the same as that between kilograms and liters.

example 1

29 parts of α, /? - di- [N-methyl-benzimidazyl- (2)] - are ethylene with 88 parts of p-Toluolsulfonsäureäthylester 8 hours at 145 to 150 ⁰ stirred. Then the mass is cooled, mixed with alcohol and allowed to cool completely. The deposited product is filtered off, washed with alcohol and dried.

549/477

C 10585 IVb / 12 p

Et, β-di- [N-methyl-N'-ethyl-N'-ptoluenesulfobenzimidazyl- (2)] -ethylene is obtained the formula

C-CH = CH-C

CH ₃

CH,

as a yellow powder that crystallizes from alcohol and so can be kept pure. The solution glows strongly when exposed to ultraviolet rays bluish.

In the above example, instead of 29 parts, α, /? - di- [N-methyl-benzimidazyl- (2)] - ethylene is used , equimolar amounts of α, / S-di- [N-benzyl-benzimidazyl- (2)] - ethylene, this gives a product that has similar properties.

If you use instead of p-toluenesulfonic acid

ethyl ester 88 parts of methyl p-toluenesulfonate, so one obtains a pale powder that is soluble in water and its solutions, ultraviolet rays exposed, glow bluish.

Example 2

The procedure is as in Example 1, but instead of a, / 3-di- [N-methylbenzimidazyl- (2)] -ethylene, a, /? -Di- [benzimidazyl- (2)] - ethylene is used.

The resulting yellow, water-soluble product of the putative formula

NH

NH

= CH-c:

O
SO ₂

CH ₃ CH ₃

has properties similar to those of Example i. It is suitable for the optical brightening of Textiles such as B. acetate rayon or cotton;

Products with similar properties are obtained if, instead of α, /? - di- [benzimidazyl- (2)] -ethylene, 6, 6'-dimethyl- or 6, ö'-dichloro-ct, ß-bi [Benzimidazyl- (2)] - ethylene quaternized in the manner indicated with ethyl p-toluenesulfonate.

Example 3

50 parts of a- [Benzimidazyl- (2)] - /? - [N-oxyäthylbenzimidazyl- (2)] - ethylene are heated ^{to 140 to 150 0 with 300 parts of dimethyl sulfate for 3 hours.} After cooling, water is added and the mixture is allowed to cool. The deposited condensation product is filtered off, washed with aqueous sodium chloride solution and dried. The yellowish powder is soluble in water with a bluish fluorescence. It can be used for the optical brightening of viscose dope.

⁸⁵ Example 4

20 parts of 1,4-di-fbenzimidazyl- (2)] benzene, 60 parts Dimethyl sulfate and 200 parts of dioxane are refluxed for 18 hours. After cooling down, the go The condensation product is filtered off, washed with dioxane and acetone and dried.

A pale powder which is soluble in water is obtained. The solution fluoresces, ultraviolet rays exposed, bluish. ,

If dibenzimidazole, a, /? - di- [benzimidazyl- (2)] -ethylene is used instead of the above, a yellowish powder with similar properties is obtained.

Example 5 ^L °°

5 parts of a, ß-di- [N-methyl-benzimidazyl- (2)] - äthylendichlorhydrat are heated with 20 parts of methanol for 15 hours in a sealed tube at 180 ° -185 ^0th After cooling, the deposited quaternary condensation product is filtered off, washed with methanol and dried.

A pale powder which is soluble in water is obtained. The solution, applied to cellulose material, glows, exposed to ultraviolet rays, bluish in color.

Example 6

200 parts of dimethyl sulfate are added to a fine suspension of 150 parts of a, β-T) i- [N-methyl-benzimidazyl- (2)] -ethylerf in 2500 parts of water over a period of 3 to 4 hours at 55 to 60 °. The temperature is then increased to 65 ° and held at this temperature for about 1 hour, a solution being formed. 375 parts of sodium chloride are then added to the solution, the precipitated condensation product is filtered off, washed with sodium chloride solution and dried. The yellow powder obtained is soluble in water with a bluish fluorescence. It can be used for the optical brightening of polyester fibers such as »Dacronee or» Terylene «.

609 54W477

: "^. ■ '■ Example 7, ■

<· '·''' ■ 40 parts ^: α, ^ -Di- [N-niethyl-benzimidazyl- (2)] - ethylene are heated with 500 parts of dioxane and 120 parts of ethyl chloride in a pressure vessel at 165 to 170 ^{0 for 24 hours} ..

After cooling, the reaction mixture is in '' ■ * · Poured water, filtered off the deposited condensation product, washed with water and removed Water crystallizes.

Yellow needles are obtained which are soluble in water are. The solution glows bluish in the ultraviolet.

Example 8

The procedure is as in Example 1, but instead of a, /? - di- [N-methyl ~ benzimide- '■''' azyi- (2)] - ethylene 2,5-di- [benzimidazyl - (2)] - furan.

The light yellow powder obtained has properties similar to those of Example i.
■ · '■. ■■■■■ ·· ■ ■

Example 9

A hot aqueous solution containing the compound obtained according to Example 2 is refluxed for 3 hours cooked and then left to cool.

The separated greenish yellow needles "'are filtered off, washed with water and dried.

The new compound of the presumed formula

CoH =

Η, α ο

CH,

has similar properties to the imidazolium compound used as the starting material.

Example 10

- A hot aqueous solution of 10 parts of the product obtained according to Example 9 is added aqueous solution of 6 parts of potassium iodide and let it cool! '

The deposited iodide of the putative formula

C ₂ H ₅

NH

CH = CH-C

is filtered off; washed with water and dried.

It forms a yellow powder with properties similar to the compound obtained in Example 9 is obtained.

The perchlorate, which has similar properties, is obtained if instead of 6 parts kali iodide, 6 parts of potassium perchlorate used.

Example 11

9 parts of α, / 3-di- [benzimidazyl- (2)] -ethylene disulfonic acid are heated with 50 parts of dimethyl sulfate for 10 hours at 140 to 150 °. Added after cooling one with alcohol, the deposited condensation product is filtered off, washed with alcohol and crystallized it from water if necessary.

The yellowish powder is more bluish in water Fluorescence soluble.

Claims (1)

PATENT CLAIM: Process for the preparation of new imidazolium compounds, characterized in that one Arylimidazoles of the composition a: .N, - R, -c: : a in which both radicals A are optionally substituted identical or different aromatic nuclei in which 2-vicinal carbon atoms are linked to the two imidazole nitrogen atoms, in which R _{1 is} hydrogen or an optionally substituted alkyl, aryl or aralkyl radical, R _{3 is} a divalent one Link with one or more conjugated double bonds, which form an uninterrupted series of conjugated double bonds with the y C = N double bonds of the imidazole rings, or the salts of these imidazoles with compounds that are able to quaternize the imidazole nitrogen atom, and possibly in known ones Way one of 2 quaternary imidazole nitrogen atoms is dequaternized again and / or the anion of the imidazolium compound is exchanged for another anion. © 609 549/477 7. 56