HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614484Generated: October 31, 2026
Benzenesulfonamide → Sodium 1-amino-4-[(benzenesulfonyl)amino]-9,10-dioxo-9,10-dihydroanthracene-2-sulfonate
https://huagongshe.com/reaction/1614484
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonamide | HCID 7370 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Lactose monohydrate | HCID 62223 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Bromamine acid sodium salt | HCID 5076555 | — |
| Catalyst | Copper sulfate pentahydrate | HCID 24463 | — |
| Solvent | Water | HCID 962 | — |
| Product | Sodium 1-amino-4-[(benzenesulfonyl)amino]-9,10-dioxo-9,10-dihydroanthracene-2-sulfonate | HCID 23672954 | 95% |
Reaction Steps
Copper (II) sulphate pentahydrate (0.16 g, 0.00064 mol) and lactose monohydrate (2.9 g, 0.008 mol) are added to a mixture of bromaminic acid sodium salt (38.2 g, 0.1 mol) and benzene sulphonamide (17.3 g, 0.11 mol) in water (250 ml) 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 5 hours. The resulting mixture is diluted with water to a volume of 750 ml 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 95% yield of 1-amino-4-phenylsulphonamido-anthraquinone-2-sulphonic acid sodium salt, a product of formula I where M denotes sodium and R denotes a group of formula III.
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-aa5311e19df3447097238bd2b0f18c4b |
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| Source note | uspto-grants-1993_03 |
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