HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 1-Bromo-4-(bromomethyl)-2-fluorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Bromo-3-fluorotoluene | HCID 573280 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1-Bromo-4-(bromomethyl)-2-fluorobenzene | HCID 11666176 | — |
Reaction Steps
A solution of 4-bromo-3-fluorotoluene (10 g, 0.053 moles) in carbon tetrachloride (100 ml) is added with N-bromosuccinimide, (NBS; 14 g, 0.08 moles). The mixture is refluxed, added with dibenzoyl peroxide (100 mg, 0.4 mmoles), refluxed for 1 hour, then cooled at room temperature and extracted with water. The aqueous phase is discarded, the organic phase is washed with brine, dried over sodium sulfate and concentrated under vacuum to give an oil (16 g) which is subjected to chromatography on a silica gel column (150 g), eluting with hexane, to afford the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022250B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-b0a0d414575c4cab82c52c6d957c444b |
| Source note | uspto-grants-2011_09 |