HuagongsheHuagongshe Chemistry Print Report · For research reference only
Anthranilic Acid → HCID 70513723, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Anthranilic Acid | HCID 227 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | HCID 70515526 | HCID 70515526 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70513723 | HCID 70513723 | — |
Reaction Steps
11.64 g (0.04 mol) of 2-(N-2-phenetylcarbamoyl)-1-naphthol was dissolved in a mixture composed of 12 g of potassium hydroxide, 25 ml of water and 200 ml of methanol. To the resulted solution, an aqueous solution of diazonium salt prepared with using 5.75 g of anthranilic acid was added to 0° to 5° C. After stirred at 5° to 10° C. for 30 minutes, 100 ml of a 20% aqueous solution of potassium hydroxide was added thereto and 50 g of sodium hydrosulfite was added at 50° to 60° C. After stirring at the same temperature for 10 minutes, it was cooled with ice and neutralized with diluted hydrochloric acid. The formed light yellow precipitate was filtered off.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04463079 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-cc5cf8ac6d9c4322a7ee200938decedc |
| Source note | uspto-grants-1984_07 |