HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-Amino-5-phenylselenophene-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-Amino-5-phenylselenophene-2-carbonitrile | HCID 86646888 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 3-Amino-5-phenylselenophene-2-carboxamide | HCID 86646887 | 67% |
Reaction Steps
To a suspension of 3-amino-5-phenylselenophene-2-carbonitrile (4.0 g) in aqueous sodium hydroxide solution (120 mL, 10%) was added ethanol (50 mL) and the mixture refluxed for 45 min. The mixture was allowed to rt and the crystals separated were filtered off, washed with cold water and dried to give the product as golden yellow color solid (2.8 g, 67%), mp 184-186° C. 1H NMR (400 MHz, CDCl3): δ 7.50-7.53 (2H, m, Ar—H), 7.36-7.38 (3H, m, Ar—H), 7.04 (1H, s, H-4), 5.84 (2H, br s, —CONH2), 5.12 (2H, br s, —NH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143237B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-9cb451e22a274ff2879b31780753d8a2 |
| Source note | uspto-grants-2012_03 |