Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,4,5,6-Tetrachloropyrimidine | HCID 15690 | — |
| Reactant | 1-Amino-4-bromo-9,10-dioxo-9,10-dihydroanthracene-2,6-disulfonic acid | HCID 9510520 | — |
| Reactant | HCID 86735077 | HCID 86735077 | — |
| Solvent | Water | HCID 962 | — |
| Product | Anthraquinone | HCID 6780 | — |
Reaction Steps
73.6 g of 1-amino-4-[3',4' -dimethyl-5'-(3"-aminophenyl-1")-disulphimido]-phenylamino-anthraquinone-2,6-disulphonic acid (produced from 1-amino-4-bromoanthraquinone-2,6-disulphonic acid and 3,3'-diamino-5,6-dimethyldibenzene-disulphimide analogously to the data in Example 1) are dissolved in 1300 ml of water and to the solution are added 22.9 g of tetrachloropyrimidine at 80°-85°. The reaction mixture is stirred at 80°-85° the reaction is completed. The pH-value is maintained at 6-7 by the addition of 20% sodium carbonate solution. As soon as the reaction is completed, the dyestuff solution is filtered and the dyestuff then precipitated by the addition of 230 g of solid sodium chloride. The dyestuff is filtered off, subsequently washed with 20% sodium chloride solution and dried in vacuo at 80°. It corresponds to the formula: ##STR35## If, instead of 1-amino-4-[3',4'-dimethyl-5'-(3"-aminophenyl-1")-disulphimido]-phenylamino-anthraquinone-2,6-disulphonic acid, equivalent amounts are used of the aminoanthraquinone dyestuffs, given in Table II, Column II, or of the stated mixtures and, instead of tetrachloropyrimidine, the acylating agents given in Column III, the procedure being otherwise as described in the example and at temperatures given in Column IV then similarly valuable blue reactive anthraquinone dyestuffs are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04049656 |
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| Source dataset | uspto-grants-1977_09 |
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| ORD ID | ord-24bf229f6bd54af2989be345d5db6ae8 |
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| Source note | uspto-grants-1977_09 |
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