HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → Phenacyl phenyl sulfide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Phenacyl phenyl sulfide | HCID 85338 | 67.7% |
Reaction Steps
To 300 mL of pyridine was added a-bromoacetophenone (150 g, 750 mmol) and thiophenol (83 g, 750 mmol). The mixture was heated at reflux for six hours. The pyridine was evaporated and the residue dissolved in ethyl acetate. The ethyl acetate solution was washed exhaustively with 1 N sodium hydroxide, then with 1 N hydrochloric acid, dried over magnesium sulfate, filtered, and evaporated to yield a brown oil. The product was crystallized from ethanol at 0° C. to yield 116 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05908859 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-a2d7cc1c6e9c4a04b436aa176967140e |
| Source note | uspto-grants-1999_06 |