HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → omega-Bromo-2-benzyloxy-acetophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-(Benzyloxy)-1-phenylethan-1-one | HCID 11253125 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | omega-Bromo-2-benzyloxy-acetophenone | HCID 20153830 | — |
Reaction Steps
Bromine (1.4 g, 8.8 mmol) is added dropwise with stirring to a solution of 2-benzyloxy-acetophenone (2.0 g, 8.8 mmol) in dry ether (30 ml) at room temperature. After stirring for additional 2 h the solution is washed with water and dried over sodium sulfate. Evaporation of the filtered solution yields the title compound. 1H-NMR (CDCl3, 400 MHz): 7.83-7.81 (m, 1H); 7.49-7.38 (m, 6H); 7.06-7.00 (m, 2H); 5.18 (s, 2H), 4.52 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08486996B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-b129e528a5e541cc8d97e01e6c55ef71 |
| Source note | uspto-grants-2013_07 |