Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Methylbenzenethiol | HCID 7811 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 23316282 | HCID 23316282 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23316291 | HCID 23316291 | 67.1% |
Reaction Steps
4.5 g of phenyl 1-amino-4,5,8-trichloroanthraquinone-2-carboxylate and 2 g of anhydrous potassium carbonate are introduced into 100 cc of dimethylformamide, 4 g of 4-methylthiophenol are added, and the mixture is then heated to 80° C. under a gentle stream of nitrogen and is kept at this temperature until the reaction is complete. The reaction mixture is then diluted at 40° C. with 40 cc of water, is allowed to cool completely and is filtered with suction, and the product is washed with a mixture of dimethylformamide and water and then with water. After drying at 60° C., 4.8 g of phenyl 1-amino-4,5,8-tri-(4-methylphenylmercapto)-anthraquinone-2-carboxylate are obtained, corresponding to a yield of 67% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04596666 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-ffe36f977f9b421da193c4de6bce4cd9 |
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| Source note | uspto-grants-1986_06 |
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