HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 7-(bromomethyl)-4-(3-fluorophenyl)-2H-chromen-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-(3-fluorophenyl)-7-methyl-2H-chromen-2-one | HCID 56971674 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 7-(bromomethyl)-4-(3-fluorophenyl)-2H-chromen-2-one | HCID 59774861 | — |
Reaction Steps
To a solution of 4-(3-fluorophenyl)-7-methyl-2H-chromen-2-one (1.25 g, 4.9 mmol) in carbontetrachloride (30 mL), N-bromosuccinimide (963 mg, 5.41 mmol) and benzoylperoxide (60 mg, 0.25 mmol) were added. The reaction was then stirred overnight at reflux. After cooling, the reaction mixture was concentrated under reduced pressure. The crude residue obtained was purified on a short column of silica gel (eluting with CH2Cl2). The filtrate was concentrated and the solid obtained was swished in a mixture of CH2Cl2/hexanes. The title product was collected by filtration. 1H NMR (400 MHz, acetone-d6): 7.72-7.6 (m, 1H), 7.55 (s, 1H), 7.47 (s, 1H), 7.45-7.3 (m, 4H), 6.4 (s, 1H), 4.78 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07960409B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-4ec1fc7ea3c547509c877eda9fe6c16d |
| Source note | uspto-grants-2011_06 |