HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Naphthylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Dinitrofluorobenzene | HCID 6264 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-1-Naphthylethylenediamine dihydrochloride | HCID 15106 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-Naphthylamine | HCID 7057 | — |
Reaction Steps
10.0 g (38.6 mmoles) of N-(1-naphthyl)-ethylenediamine dihydrochloride were dissolved in a little water and neutralized with dilute sodium hydroxide solution. After the addition of 120 ml of ethanol and 6.4 g of potassium carbonate (46.3 mmoles), 7.2 g (38.7 mmoles) of 2,4-dinitrofluorobenzene were added dropwise. After refluxing for 1 hour, the whole was cooled to room temperature and the deposit was filtered off under suction and washed with water/ethanol. The intermediate product (2-(2,4-dinitrophenyl)-amino)-ethyl)-naphthylamine was obtained in the form of red crystals with a melting point of 263° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06828443B1 |
| Source dataset | uspto-grants-2004_12 |
| ORD ID | ord-d6b9a224570e4d0eb3409899f20c935a |
| Source note | uspto-grants-2004_12 |