HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-2'-nitroacetophenone → 4-(2-Nitrophenyl)thiazole-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-2'-nitroacetophenone | HCID 244025 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(2-Nitrophenyl)thiazole-2-amine | HCID 595779 | — |
Reaction Steps
4-(2-Nitro-phenyl)-thiazol-2-ylamine was prepared as follows: 2-Bromo-2′-nitroacetophenone (1.75 g, 7.2 mmol) was mixed with 50 mL of absolute EtOH along with thiourea (1.09 g, 14.4 mmol) and stirred under reflux for 2 hours. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The resulting residue was basified with 20 mL of 1 N aqueous NaOH and extracted with CH2Cl2. The combined organic layers were dried (Na2SO4) and concentrated to afford essentially quantitative yield of 4-(2-nitro-phenyl)-thiazol-2-ylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088928B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-f45d86eaa3234b0bbb13b75f84f29e24 |
| Source note | uspto-grants-2012_01 |