HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromophenacyl bromide → 2-azido-1-(4-bromophenyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromophenacyl bromide | HCID 7454 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-azido-1-(4-bromophenyl)ethanone | HCID 11021004 | 83.4% |
Reaction Steps
A solution of 2,4′-dibromoacetophenone (1.390 g, 5.0 mmol) in MeOH (10 mL) was poured over 10 mL of an aqueous solution of sodium azide (0.325 g, 5.00 mmol) in an ice bath. The mixture was stirred at room temperature for 18 hours. The solvent was removed and then extracted with ethyl ether (20 mL) and water (20 mL). The organic layer was dried over MgSO4 and concentrated in vacuo to obtain 2-azido 4′-bromoacetophenone (1.0 g, 4.17 mmol, 83% yield). 1H NMR (CDCl3) 5.45 (s, 2H), 7.67 (d, J=8.4 Hz, 2H), 7.79 (d, J=8.4 Hz, 2H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08394742B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-c913f17f6b9e443bada90e6eade854b3 |
| Source note | uspto-grants-2013_03 |