HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614483Generated: November 3, 2026
P-Toluenesulfonamide → HCID 131717833, compound
https://huagongshe.com/reaction/1614483
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Toluenesulfonamide | HCID 6269 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Bromamine acid sodium salt | HCID 5076555 | — |
| Reactant | Glucose Monohydrate | HCID 22814120 | — |
| Catalyst | Cupric acetate monohydrate | HCID 165397 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131717833 | HCID 131717833 | 97% |
Reaction Steps
Copper (II) acetate monohydrate (0.13 g, 0.00064 mol) and glucose monohydrate (1.6 g, 0.008 mol) are added to a mixture of bromaminic acid sodium salt (38.2 g, 0.1 mol) and p-toluenesulphonamide (18.8 g 0.11 mol) in water (250 mol) containing sodium carbonate (3.8 g) and sodium bicarbonate (19.0 g). The mixture which has a pH of 8.5-9.0, is heated to 70° C. and stirred at this temperature for five hours. The resulting mixture is diluted to a volume of 750 ml with water and cooled to 40° C. The solid product is filtered off and washed with a solution of sodium chloride (12 g) in water (1300 ml) to give a 97% yield 1-amino-4-(4'-methlylphenylsulphonamido)-anthraquinone-2-sulphonic acid sodium salt, a product of formula I where M denotes sodium and R denotes a group of formula IV.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05196553 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-28b472b8e83b40bbaf214a7ecca04933 |
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| Source note | uspto-grants-1993_03 |
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