HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → 7-(bromomethyl)-5-fluoro-2,2-dimethylbenzofuran-3(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-fluoro-2,2,7-trimethylbenzofuran-3(2H)-one | HCID 58566299 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 7-(bromomethyl)-5-fluoro-2,2-dimethylbenzofuran-3(2H)-one | HCID 58566723 | — |
Reaction Steps
A solution of provide 5-fluoro-2,2,7-trimethylbenzofuran-3(2H)-one (659) (100 mg, 0.515 mmol), N-Bromosuccinimide (100.8 mg, 0.567 mmol), benzoyl chloride (1.2 mg, 0.005 mmol) and carbon tetrachloride (2 mL) was heated at reflux overnight. Saturated sodium bicarbonate was added and extracted with ethyl acetate, dried over sodium sulfate, filtered and concentrated in vacuo. The crude compound was purified by flash column chromatography on silica gel with hexanes and EtOAc (5%) to give 7-(bromomethyl)-5-fluoro-2,2-dimethylbenzofuran-3(2H)-one (660).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598374B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-a020fb646b1a407b9ce4dda8b5fe42ad |
| Source note | uspto-grants-2013_12 |