HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210623Generated: October 26, 2026
3-Aminobenzenesulfonic acid → 2-Amino-1,5-naphthalenedisulfonic acid
https://huagongshe.com/reaction/2210623
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Aminobenzenesulfonic acid | HCID 8474 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Amino-5-hydroxynaphthalene-1,7-disulphonic acid | HCID 81024 | — |
| Reactant | 4,5,6-Trifluoro-1,2,3-triazine | HCID 13899144 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-1,5-naphthalenedisulfonic acid | HCID 8338 | 100% |
Reaction Steps
31.9 g of 2-amino-5-hydroxynaphthalene-1,7-disulphonic acid are dissolved in 400 ml of water under neutral conditions. 300 g of ice are then added, and 8.8 ml of trifluorotriazine are run in while maintaining a pH of 4.0 to 4.5 with 15% strength sodium carbonate solution. Stirring is continued for 5 minutes, and a neutral solution of 17.3 g of m-sulphanilic acid is then added while maintaining a pH of 5.0 to 5.5 with 15% strength sodium carbonate solution. During acylation, the temperature is allowed to rise to 15° to 20°. A diazo compound obtained in the usual manner by diazotisation of 30.3 g of 2-aminonaphthalene-1,5-disulphonic acid is added to the resulting solution of the reaction product of the formula ##STR15## at 5° to 10°, while simultaneously maintaining the pH at 7.0 to 7.5 by sprinkling in sodium bicarbonate. After coupling is complete, the dyestuff of the formula ##STR16## is salted out, filtered off with suction, dried and milled.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05459245 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-99e5f17fa37448a69ea6137be3748fa9 |
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| Source note | uspto-grants-1995_10 |
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