HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 2-Bromo-1-phenyl-2-(phenylthio)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Phenacyl phenyl sulfide | HCID 85338 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Bromo-1-phenyl-2-(phenylthio)ethanone | HCID 15651235 | 100% |
Reaction Steps
To a solution of 1-phenyl-2-(phenylthio)ethanone (2.1 g) in acetic acid (20 mL) was added bromine (0.5 mL) and the mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated under reduced pressure, water was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate solution, water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give the title compound as a yellow oil (yield 2.9 g, yield about 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08334301B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-9a647a8988294851975839e76f87ccc1 |
| Source note | uspto-grants-2012_12 |