HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 6-Bromo-3-(bromomethyl)benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 2-(2-acetyl-5-bromophenoxy)acetate | HCID 57419482 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 6-Bromo-3-(bromomethyl)benzofuran | HCID 57419483 | 32% |
Reaction Steps
A solution of the product from Example 88, Part C (1.0 g, 4.74 mmol) and dibenzoyl peroxide (287 mg, 1.19 mmol) in chlorobenzene (24 mL) at reflux was treated in four portions with N-bromosuccinimide (843 mg, 4.74 mmol) over 30 min. The mixture was then stirred at reflux for 2 h. The mixture was cooled, filtered and concentrated and purified by column chromatography on silica gel, eluting with 7-30% chloroform in hexanes. The procedures afforded the title compound as a light yellow oil (438 mg, 32%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09095590B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-cf9d4e94391742038d03178e5a45ea56 |
| Source note | uspto-grants-2015_08 |