HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Ethanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4'-Hydroxy-3'-methylacetophenone | HCID 70135 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]- | HCID 12969325 | 99.1% |
Reaction Steps
A mixture of 4′-hydroxy-3′-methylacetophenone (10.00 g; 66.6 mmol) and K2CO3 (13.80 g; 99.9 mmol) in acetone (100 mL) was stirred, at RT for 40 minutes. Subsequently, benzyl bromide (7.9 mL; 66.6 mmol) was added and the resulting mixture was heated under reflux for 2.5 h. After cooling to RT the mixture was concentrated in vacuo. The residue was dissolved in EtOAc, washed with 5% aqueous ammonia, water, and brine, dried (MgSO4), filtered and concentrated in vacuo to afford 1-(4-benzyloxy-3-methylphenyl)-ethanone (15.86 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273017B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-5a70cc3c54f4465b9e8c3febbea89ff0 |
| Source note | uspto-grants-2016_03 |