HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → HCID 59658556, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Mercaptobenzoic acid | HCID 95738 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59658556 | HCID 59658556 | — |
Reaction Steps
To bromoacetophenone (322.8 mg, 1.62 mmole) and anhydrous K2CO3 (896 mg, 6.48 mmole) in ethanol (20 ml), 250 mg (1.62 mmole) 4-mercaptobenzoic acid was added and the mixture refluxed overnight. The solvent was evaporated and water added to the solid residue. The basic aqueous solution was extracted with ethyl acetate to remove unreacted bromoacetophenone. The aqueous layer was acidified to yield a precipitate which was filtered and dried (356 mg). m/z 271 (M−1)+. 1H NMR (DMSO) δ 4.75 (2H, s, —CH2-), 7.35-7.72 (5H, m, 5×ArH), 7.82 (2H, d, 2×ArH), 8.05 (2H, d, 2×ArH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07910770B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-1697958144e2488f9b0db50ddf72af57 |
| Source note | uspto-grants-2011_03 |