HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 1,3-Dibromo-2-(bromomethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | 2,6-Dibromotoluene | HCID 34681 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1,3-Dibromo-2-(bromomethyl)benzene | HCID 13381015 | — |
Reaction Steps
To the solution of 2,6-dibromotoluene (55.5 g, 222.1 mmol) and NBS (43.5 g, 244.3 mmol) in carbon tetrachloride (300 mL) was added benzoyl peroxide (5.37 g, 22.2 mmol). The reaction mixture was refluxed for 20 h, cooled to room temperature, washed with water (300 mL×3) and brine (300 mL) and dried over anhydrous sodium sulfate. The solution was filtered and evaporated to give 1,3-dibromo-2-bromomethylbenzene as a yellow power (71 g). This material was used for next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08729078B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-118bf696674346bf91f4652946012bfb |
| Source note | uspto-grants-2014_05 |