HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Nitronaphthalene → 4-Nitro-1-naphthylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Nitronaphthalene | HCID 6849 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-Nitro-1-naphthylamine | HCID 13057 | — |
Reaction Steps
3.5 g of 1-nitronaphthalene and 3.3 g of N,N-tetramethylenethiocarbamoylsulphenamide, dissolved in 15 ml of dimethyl sulphoxide, are added dropwise to a vigorously stirred suspension of 6 g of potassium hydroxide in 50 ml of dimethyl sulphoxide, the temperature being kept at 20° to 25° C. When the addition has ended the mixture is stirred for a further 60 minutes, poured into 400 ml of a saturated aqueous ammonium chloride solution and extracted with methylene chloride. After drying and removing the solvent, 4-nitro-1-naphthylamine is obtained with a melting point of 190° to 192° C. The yield is 2.9 g (77%). 1Nitro-2-napthylamine is additionally obtained in a yield of about 2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05262539 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-7974db6dad9b4a9cad76e2dd880c957c |
| Source note | uspto-grants-1993_11 |