HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 2-Bromo-4-(bromomethyl)-1-methoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Bromo-4-methylanisole | HCID 89143 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Product | 2-Bromo-4-(bromomethyl)-1-methoxybenzene | HCID 11277462 | 100% |
Reaction Steps
2-Bromo-4-methyl anisole 14 (2.2 mL, 14.9 mmol) was dissolved in dichlomethane (30 mL) and N-bromosuccinimide (3.75 g, 16.4 mmol) was added followed by AIBN (26.0 mg). The reaction was heated to reflux for 19 hrs., then cooled to room temperature and the precipitate was filtered off. The filtrate was diluted with dichloromethane and washed with 0.5 M aqueous sodium bicarbonate, followed by water. The organic mixture was dried over sodium sulfate, filtered and concentrated under vacuum to yield 15 (4.16 g, 100%). The benzyl bromide was used as the crude material without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531544B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-5109376a568e483292ffa4820f2aa5f8 |
| Source note | uspto-grants-2009_05 |