HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromophenacyl bromide → 4-(4-Bromophenyl)-1,3-oxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromophenacyl bromide | HCID 7454 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 4-(4-Bromophenyl)-1,3-oxazole | HCID 22316595 | 26% |
Reaction Steps
To a stirred solution of 2,4′-dibromoacetophenone (9.66 g, 34.8 mmol) in formic acid (42 ml) was added ammonium formate (7.58 g, 120.6 mmol), and the mixture was heated at reflux temperature for 3 hours. The reaction mixture was cooled down to room temperature, and made basic by addition of 50% NaOH aqueous solution. The whole was extracted with CH2H2. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography eluting with ethyl acetate-hexane (1:5) to give title compound (2.0 g, 26% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06608095B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-f516d7b7f34141a8b7cf9f8f61d59064 |
| Source note | uspto-grants-2003_08 |