HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-METHYLACETOPHENONE → 2-Bromo-4'-methylacetophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-METHYLACETOPHENONE | HCID 8500 | — |
| Reactant | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | 2-Bromo-4'-methylacetophenone | HCID 69272 | 84% |
Reaction Steps
To a solution of 1-p-tolyl-ethanone (0.5 g, 4.16 mmol) in dichloromethane-methanol (50 ml-20 mL) was added tetrabutylammonium tribromide (2.2 g, 4.58 mmol) at room temperature. The mixture was stirred until the orange color faded. The solvent was then distilled under reduced pressure and the resulting precipitate was extracted with ethyl acetate. The organic layer was dried over sodium sulfate and evaporated in vacuo to give a residue which was purified by flash column chromatography to yield the desired product 2-bromo-1-p-tolyl-1-ethanone (0.74 g, 84%). 1H NMR (300 MHz, DMSO-d6) δ 2.39 (s, 3H), 4.89 (s, 2H), 7.37 (d, 2H), 7.89 (d, 2H); ESI-MS (MH+): 213 and 215.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772248B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-a9b151c6b0a743549ed15e2759fde192 |
| Source note | uspto-grants-2010_08 |