HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 1-[3-Bromo-4-(bromomethyl)-5-chloro-2-methoxyphenyl]ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-(3-Bromo-5-chloro-2-methoxy-4-methylphenyl)ethanone | HCID 86666759 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1-[3-Bromo-4-(bromomethyl)-5-chloro-2-methoxyphenyl]ethanone | HCID 86666765 | — |
Reaction Steps
A mixture of 1-(3-bromo-5-chloro-2-methoxy-4-methylphenyl)ethanone (3.3 g, 12 mmol), N-bromosuccinimide (2.2 g, 13 mmol), and benzoyl peroxide (0.15 g, 0.60 mmol) in carbon tetrachloride (50 mL) was heated at reflux overnight. The mixture was cooled to room temperature and concentrated. The resulting residue was diluted with ethyl acetate and washed with water. The organic layers were dried over magnesium sulfate and evaporated to dryness. The crude product was used directly in next step. LCMS calculated for C10H10Br2ClO2 (M+H)+: m/z=355.1. found: 355.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096600B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-fe69af24a12f4c9b90fea368797324c4 |
| Source note | uspto-grants-2015_08 |