HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Dibromotoluene → 3,5-Dibromobenzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Dibromotoluene | HCID 15361 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3,5-Dibromobenzyl bromide | HCID 143427 | 44% |
Reaction Steps
3,5-dibromotoluene (78.92 g, 0.316 mole) was dissolved in 1.27 L of carbon tetrachloride; to this solution was added N-bromosuccinimide (61.65 g, 0.346 mole) at room temperature. A portion of dibenzoyl peroxide (0.6 g, 0.008 equivalents) was added and the solution heated to reflux temperature for 2.5 hours. The reaction mixture was cooled to room temperature, filtered and the solvent removed in vacuo to yield a solid. The solid was dissolved in 200 mL of warm hexane, filtered and cooled to room temperature. Crystallizations ensued; the crystals were filtered off and washed with cold hexane and air dried to give 45.15 g (44%) of 3,5-dibromobenzyl bromide. 1H-NMR(CDCl3); δ7.6 (1H), 7.47 (2H), 4.36 (2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05541319 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-9a6f6b39c8ef4c37959f36b46c4d8d9f |
| Source note | uspto-grants-1996_07 |