Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfanilamide | HCID 5333 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 2-Naphthalenecarboxylic acid, 1-hydroxy-4-nitro-, phenyl ester | HCID 103329 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 54068405 | HCID 54068405 | — |
Reaction Steps
A mixture composed of 30.9 g (0.1 mol) of phenyl 1-hydroxy-4-nitro-2-naphthoate, 17.2 g of p-aminobenzenesulfonamide and 200 ml of diethylene glycol dimethyl ether was heated at 160° C. for 3 hours. After cooling, the separated yellow crystals were filtered off. Yield: 19 g. 7.74 g (0.02 mol) of the resulting yellow crystals were dissolved in 100 ml of 10% sodium hydroxide. Then 40 g of sodium hydrosulfite was added at 50° to 60° C. thereto. After stirring at the same temperature for 30 minutes, the solution was allowed to cool and neutralized with diluted hydrochloric acid. The resulting light yellow precipitate of (4-a) was filtered off. Yield: 5.3 g
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04463079 |
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| Source dataset | uspto-grants-1984_07 |
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| ORD ID | ord-dbe0ab8b195647b99e2d5ddf8d8f4d11 |
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| Source note | uspto-grants-1984_07 |
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