Claims
- 1. A process for the preparation of 4,4'-dinitrostilbene-2,2'-disulfonic acid, or salt thereof, of the formula ##STR7## in which M is hydrogen or an alkali metal cation, which process comprises: a. oxygenating a reaction medium comprising:
- (i) a solvent selected from the group consisting of N-methylpyrrolidone; dimethylsulfoxide; sulfolane; acetonitrile; tetramethylurea; aprotic dipolar solvents of the formula ##STR8## wherein R is a C.sub.1 -C.sub.4 -alkyl group, R.sub.1 is a C.sub.1 -C.sub.4 -carboxylic acid or phosphoric acid radical, w is the basicity of the acid and the v's are 0, 1, or 2; and mixtures thereof, which solvent or solvent mixture is pure or combined with one or more C.sub.1 -C.sub.4 alcohols;
- (ii) a catalytically-effective amount of a catalyst selected from the group consisting of salts, oxides, hydroxides and organic compounds of heavy metals; inorganic or organic bromine or iodine compounds; and phase transfer catalysts; and
- (iii) a catalytically effective amount of a strongly basic compound of aluminum, an alkali metal or an alkaline earth; or strongly basic ion exchanger; or mixture of any or all of these;
- b. dissolving 4-nitro-2-toluene sulfonic acid or alkali metal salt thereof in a solvent of step (a-i); and
- c. combining the solution of step (b) with the reaction medium of step (a) while continuously oxygenating the resulting mixture.
- 2. A process according to claim 1 wherein the catalyst is a salt, oxide, hydroxide or organic compound of manganese.
- 3. A process according to claim 1 wherein the aprotic dipolar solvent is dimethylformamide, diethylformamide, hexamethylphosphoric acid triamide, dimethylacetamide or diethylacetamide.
- 4. A process according to claim 3 wherein the solvent of step (a-l) is a mixture of dimethylformamide and methanol, diethylformamide and methanol, or dimethylformamide and diethylformamide and methanol.
- 5. A process according to claim 4 wherein said strongly basic compound is a hydroxide, amide, hydride, alcoholate, sulfide, or mixture thereof.
- 6. A process according to claim 5 wherein said strongly basic compound is a hydroxide, amide or alcoholate of potassium or sodium.
- 7. A process according to claim 1 wherein the strongly basic compound is used in an at least equivalent amount.
- 8. A process according to claim 1 wherein step (c) is conducted at a temperature of 0.degree. C. to 25.degree. C.
- 9. A process according to claim 1 wherein said catalyst is a phase transfer catalyst.
- 10. A process according to claim 1 wherein said oxygenating is effected with air, pure oxygen, or a mixture of oxygen with inert gas.
- 11. A process according to claim 1 wherein oxygenating is effected at supraatmospheric pressure.
- 12. A process for the preparation of 4,4'-dinitrostilbene-2,2'-disulfonic acid, or salt thereof, of the formula ##STR9## in which M is hydrogen or an alkali metal cation, which process comprises: a. oxygenating a reaction medium comprising:
- (i) a solvent selected from the group consisting of N-methylpyrrolidone; dimethylsulfoxide; sulfolane; acetonitrile; tetramethylurea; aprotic dipolar solvents of the formula ##STR10## wherein R is a C.sub.1 -C.sub.4 -alkyl group, R.sub.1 is a C.sub.1 -C.sub.4 -carboxylic acid or phosphoric acid radical, w is the basicity of the acid and the v's are 0, 1, or 2; and mixtures thereof, which solvent or solvent mixture is pure or combined with one or more C.sub.1 -C.sub.4 alcohols;
- (ii) a catalytically effective amount of a manganese salt, oxide, hydroxide or organic compound; and
- (iii) a catalytically effective amount of a strongly basic compound of aluminum, an alkali metal or an alkaline earth; or strongly basic ion exchanger; or mixture of any or all of these;
- b. dissolving 4-nitro-2-toluene sulfonic acid or alkali metal salt thereof in a solvent of step (a-i); and
- c. adding the solution of step (b) to the reaction medium of step (a) while continuously oxygenating the resulting mixture.
- 13. A process according to claim 12 wherein said manganese salt is manganese (II) sulfate or nitrate and is used in an amount that is 0.1 to 15 percent by weight of the amount of 4-nitro-2-toluene sulfonic acid.
- 14. A process according to claim 13 wherein said aprotic dipolar solvent is dimethylformamide, hexamethylphosphoric acid triamide, dimethylformamide or diethylacetamide, dimethylacetamide or a mixture of any or all of these.
- 15. A process according to claim 13 wherein said strongly basic compound is a hydroxide, amide, hydride, alcoholate or sulfide of potassium or sodium, or mixture thereof and is used in an amount at least equivalent to the amount of 4-nitro-2-toluene sulfonic acid.
Priority Claims (1)
Number |
Date |
Country |
Kind |
5369/79 |
Jun 1979 |
CHX |
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Parent Case Info
This application is a continuation of application Ser. No. 782,617, filed Oct. 1, 1985, which is a continuation of Ser. No. 699,496, filed Feb. 8, 1985, which is a continuation of Ser. No. 294,954, filed Aug. 21, 1981 which is a continuation of Ser. No. 154,338, filed May 29, 1980, all abandoned.
US Referenced Citations (2)
Number |
Name |
Date |
Kind |
2212084 |
Straub et al. |
Aug 1940 |
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2821550 |
Strobel |
Jan 1958 |
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Non-Patent Literature Citations (9)
Entry |
Journal of Organic Chem., vol. 32, pp. 137-146 (Jan., 1967). |
Chemical Abstracts, vol. 83, 1975. |
Chemical Abstract, vol. 84, 1976. |
Miyata et al., Chem Abst., vol. 83, 113377k (1975). |
Kompolshy et al., Chem Abst., vol. 84, 58886u (1976). |
Glen A. Russell et al.; J. Am. Chem. Soc., vol. 84, pp. 4153-4154 (1962). |
Glen A. Russell et al.,--J. Am. Chem. Soc., vol. 88, pp. 5491-5497 (1966). |
Glen A. Russell et al.; J. Am. Chem. Soc., vol. 89, pp. 300-308, (1967). |
Glen A. Russell et al.; J. Org. Chem., vol. 32, pp. 137-146 (1967). |
Continuations (4)
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Number |
Date |
Country |
Parent |
782617 |
Oct 1985 |
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Parent |
699496 |
Feb 1985 |
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Parent |
294954 |
Aug 1981 |
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Parent |
154338 |
May 1980 |
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