HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → 2-(2-Bromophenoxy)-1-phenylethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | 2-Bromophenol | HCID 7244 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(2-Bromophenoxy)-1-phenylethan-1-one | HCID 3016354 | — |
Reaction Steps
To a solution of 2-bromophenol (8.71 g; 50.3 mmol) and bromoacetophenone (10.1 g; 50.5 mmol) in 50 ml acetone was added K2CO3 (7.02 g; 50.8 mmol). The mixture was heated to reflux for 10 h, cooled to r.t., filtered, diluted with EtOAc (100 ml), washed with HCl (1.0 M, 2×100 ml) and brine, dried over MgSO4 and concentrated. The residual solid was recrystallized from EtOAc:hexane to afford the desired material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211197B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-e8ea565d4667442bad8a8029ce85b129 |
| Source note | uspto-grants-2001_04 |